| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001126128.1 | 392 | Missense Mutation | CGG,TGG | R101W | NP_001119600.1 |
| NM_021935.3 | 392 | Missense Mutation | CGG,TGG | R80W | NP_068754.1 |
| XM_017006974.1 | 392 | Missense Mutation | CGG,TGG | R81W | XP_016862463.1 |