Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_006329.3 | 1753 | Missense Mutation | ACG,ATG | T397M | NP_006320.2 |
XM_005267267.3 | 1753 | Missense Mutation | ACG,ATG | T414M | XP_005267324.1 |
XM_011536356.1 | 1753 | Missense Mutation | CGG,TGG | R474W | XP_011534658.1 |
XM_011536357.1 | 1753 | Missense Mutation | CGG,TGG | R457W | XP_011534659.1 |
XM_011536358.1 | 1753 | Missense Mutation | CGG,TGG | R401W | XP_011534660.1 |
XM_017020929.1 | 1753 | Missense Mutation | ACG,ATG | T341M | XP_016876418.1 |