| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_207385.1 | 2162 | Missense Mutation | CGG,TGG | R98W | NP_997268.1 |
| XM_017023228.1 | 2162 | Missense Mutation | CGG,TGG | R98W | XP_016878717.1 |
| XM_017023229.1 | 2162 | Missense Mutation | CGG,TGG | R98W | XP_016878718.1 |