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SNP ID Transcript ID Gene Name: Consequence Type BioType Protein ID Protein Position Residue Change
cfa11039093 ENSCAFT00000028993 ENSCAFG00000018251:NMD_transcript_variant protein_coding ENSCAFP00000026963 - -
cfa11039093 ENSCAFT00000069213 ENSCAFG00000018251:NMD_transcript_variant protein_coding ENSCAFP00000056751 - -
cfa11039093 ENSCAFT00000075651 ENSCAFG00000018251:NMD_transcript_variant protein_coding ENSCAFP00000059935 - -
cfa11039094 ENSCAFT00000028993 ENSCAFG00000018251:NMD_transcript_variant protein_coding ENSCAFP00000026963 - -
cfa11039094 ENSCAFT00000069213 ENSCAFG00000018251:NMD_transcript_variant protein_coding ENSCAFP00000056751 - -
cfa11039094 ENSCAFT00000072299 ENSCAFG00000018251:NMD_transcript_variant protein_coding ENSCAFP00000048272 - -
cfa11039094 ENSCAFT00000075651 ENSCAFG00000018251:NMD_transcript_variant protein_coding ENSCAFP00000059935 - -
cfa11039095 ENSCAFT00000028993 ENSCAFG00000018251:NMD_transcript_variant protein_coding ENSCAFP00000026963 - -
cfa11039095 ENSCAFT00000069213 ENSCAFG00000018251:NMD_transcript_variant protein_coding ENSCAFP00000056751 - -
cfa11039095 ENSCAFT00000072299 ENSCAFG00000018251:NMD_transcript_variant protein_coding ENSCAFP00000048272 - -
cfa11039095 ENSCAFT00000075651 ENSCAFG00000018251:NMD_transcript_variant protein_coding ENSCAFP00000059935 - -
cfa11039096 ENSCAFT00000028993 ENSCAFG00000018251:NMD_transcript_variant protein_coding ENSCAFP00000026963 - -
cfa11039096 ENSCAFT00000069213 ENSCAFG00000018251:NMD_transcript_variant protein_coding ENSCAFP00000056751 - -
cfa11039096 ENSCAFT00000072299 ENSCAFG00000018251:NMD_transcript_variant protein_coding ENSCAFP00000048272 - -
cfa11039096 ENSCAFT00000075651 ENSCAFG00000018251:NMD_transcript_variant protein_coding ENSCAFP00000059935 - -