| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001204414.1 | 211 | Missense Mutation | CGG,TGG | R29W | NP_001191343.1 |
| NM_001204415.1 | 211 | Intron | NP_001191344.1 | ||
| NM_022164.2 | 211 | Missense Mutation | CGG,TGG | R29W | NP_071447.1 |
| XM_005271106.2 | 211 | Missense Mutation | CGG,TGG | R29W | XP_005271163.1 |
| XM_005271107.2 | 211 | Intron | XP_005271164.1 | ||
| XM_011541946.1 | 211 | Intron | XP_011540248.1 |