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SNP ID Transcript ID Gene Name: Consequence Type BioType Protein ID Protein Position Residue Change
cfa39127766 ENSCAFT00000049014 ENSCAFG00000007131:NMD_transcript_variant protein_coding ENSCAFP00000039976 - -
cfa39127767 ENSCAFT00000049014 ENSCAFG00000007131:NMD_transcript_variant protein_coding ENSCAFP00000039976 - -
cfa39127768 ENSCAFT00000049014 ENSCAFG00000007131:NMD_transcript_variant protein_coding ENSCAFP00000039976 - -
cfa39127769 ENSCAFT00000049014 ENSCAFG00000007131:NMD_transcript_variant protein_coding ENSCAFP00000039976 - -
cfa39127770 ENSCAFT00000049014 ENSCAFG00000007131:NMD_transcript_variant protein_coding ENSCAFP00000039976 - -
cfa39127771 ENSCAFT00000049014 ENSCAFG00000007131:NMD_transcript_variant protein_coding ENSCAFP00000039976 - -
cfa39127772 ENSCAFT00000049014 ENSCAFG00000007131:NMD_transcript_variant protein_coding ENSCAFP00000039976 - -
cfa39127773 ENSCAFT00000049014 ENSCAFG00000007131:NMD_transcript_variant protein_coding ENSCAFP00000039976 - -
cfa39127774 ENSCAFT00000049014 ENSCAFG00000007131:NMD_transcript_variant protein_coding ENSCAFP00000039976 - -
cfa39127775 ENSCAFT00000049014 ENSCAFG00000007131:NMD_transcript_variant protein_coding ENSCAFP00000039976 - -
cfa39127776 ENSCAFT00000049014 ENSCAFG00000007131:NMD_transcript_variant protein_coding ENSCAFP00000039976 - -
cfa39127777 ENSCAFT00000049014 ENSCAFG00000007131:NMD_transcript_variant protein_coding ENSCAFP00000039976 - -
cfa39127778 ENSCAFT00000049014 ENSCAFG00000007131:NMD_transcript_variant protein_coding ENSCAFP00000039976 - -
cfa39127779 ENSCAFT00000049014 ENSCAFG00000007131:NMD_transcript_variant protein_coding ENSCAFP00000039976 - -
cfa39127780 ENSCAFT00000049014 ENSCAFG00000007131:NMD_transcript_variant protein_coding ENSCAFP00000039976 - -