| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001270891.1 | 397 | Silent Mutation | TGC,TGT | C124C | NP_001257820.1 |
| NM_001270892.1 | 397 | Missense Mutation | CGG,TGG | R116W | NP_001257821.1 |
| NM_001270893.1 | 397 | Missense Mutation | CGG,TGG | R102W | NP_001257822.1 |
| NM_024108.2 | 397 | Silent Mutation | TGC,TGT | C138C | NP_077013.1 |
| XM_017027295.1 | 397 | Missense Mutation | CGG,TGG | R151W | XP_016882784.1 |