| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001319945.1 | 865 | Missense Mutation | CGG,TGG | R136W | NP_001306874.1 |
| NM_138387.3 | 865 | Missense Mutation | CGG,TGG | R136W | NP_612396.1 |
| XM_011525473.2 | 865 | Missense Mutation | CGG,TGG | R21W | XP_011523775.1 |
| XM_011525474.2 | 865 | Missense Mutation | CGG,TGG | R21W | XP_011523776.1 |
| XM_017025335.1 | 865 | Missense Mutation | CGG,TGG | R21W | XP_016880824.1 |