Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001257370.1 | 511 | Missense Mutation | CGG,TGG | R197W | NP_001244299.1 |
XM_017023025.1 | 511 | Missense Mutation | CGG,TGG | R169W | XP_016878514.1 |
XM_017023026.1 | 511 | Missense Mutation | CGG,TGG | R166W | XP_016878515.1 |