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SNP ID Transcript ID Gene Name: Consequence Type BioType Protein ID Protein Position Residue Change
cfa39127751 ENSCAFT00000049014 ENSCAFG00000007131:NMD_transcript_variant protein_coding ENSCAFP00000039976 - -
cfa39127752 ENSCAFT00000049014 ENSCAFG00000007131:NMD_transcript_variant protein_coding ENSCAFP00000039976 - -
cfa39127753 ENSCAFT00000049014 ENSCAFG00000007131:NMD_transcript_variant protein_coding ENSCAFP00000039976 - -
cfa39127754 ENSCAFT00000049014 ENSCAFG00000007131:NMD_transcript_variant protein_coding ENSCAFP00000039976 - -
cfa39127755 ENSCAFT00000049014 ENSCAFG00000007131:NMD_transcript_variant protein_coding ENSCAFP00000039976 - -
cfa39127756 ENSCAFT00000049014 ENSCAFG00000007131:NMD_transcript_variant protein_coding ENSCAFP00000039976 - -
cfa39127757 ENSCAFT00000049014 ENSCAFG00000007131:NMD_transcript_variant protein_coding ENSCAFP00000039976 - -
cfa39127758 ENSCAFT00000049014 ENSCAFG00000007131:NMD_transcript_variant protein_coding ENSCAFP00000039976 - -
cfa39127759 ENSCAFT00000049014 ENSCAFG00000007131:NMD_transcript_variant protein_coding ENSCAFP00000039976 - -
cfa39127760 ENSCAFT00000049014 ENSCAFG00000007131:NMD_transcript_variant protein_coding ENSCAFP00000039976 - -
cfa39127761 ENSCAFT00000049014 ENSCAFG00000007131:NMD_transcript_variant protein_coding ENSCAFP00000039976 - -
cfa39127762 ENSCAFT00000049014 ENSCAFG00000007131:NMD_transcript_variant protein_coding ENSCAFP00000039976 - -
cfa39127763 ENSCAFT00000049014 ENSCAFG00000007131:NMD_transcript_variant protein_coding ENSCAFP00000039976 - -
cfa39127764 ENSCAFT00000049014 ENSCAFG00000007131:NMD_transcript_variant protein_coding ENSCAFP00000039976 - -
cfa39127765 ENSCAFT00000049014 ENSCAFG00000007131:NMD_transcript_variant protein_coding ENSCAFP00000039976 - -