| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_003807.4 | 965 | Missense Mutation | CGG,TGG | R195W | NP_003798.2 |
| NM_172014.3 | 965 | Missense Mutation | CGG,TGG | R159W | NP_742011.2 |
| XM_017027417.1 | 965 | Missense Mutation | CGG,TGG | R195W | XP_016882906.1 |
| XM_017027418.1 | 965 | Intron | XP_016882907.1 |