Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
XM_005256013.2 | 659 | Missense Mutation | CTT,TTT | L161F | XP_005256070.1 |
XM_011523188.2 | 659 | Missense Mutation | CTT,TTT | L130F | XP_011521490.1 |
XM_017023385.1 | 659 | Missense Mutation | CTT,TTT | L16F | XP_016878874.1 |
XM_017023386.1 | 659 | Missense Mutation | CTT,TTT | L16F | XP_016878875.1 |