Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
XM_017012174.1 | 2728 | Missense Mutation | CGG,TGG | R363W | XP_016867663.1 |
XM_017012175.1 | 2728 | Missense Mutation | CGG,TGG | R298W | XP_016867664.1 |
XM_017012176.1 | 2728 | Missense Mutation | CGG,TGG | R241W | XP_016867665.1 |