| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001168298.1 | 124 | Missense Mutation | CGG,TGG | R15W | NP_001161770.1 |
| NM_001557.3 | 124 | Missense Mutation | CGG,TGG | R15W | NP_001548.1 |
| XM_005246530.3 | 124 | Intron | XP_005246587.1 | ||
| XM_017003990.1 | 124 | Missense Mutation | CGG,TGG | R15W | XP_016859479.1 |
| XM_017003991.1 | 124 | Missense Mutation | CGG,TGG | R15W | XP_016859480.1 |
| XM_017003992.1 | 124 | Missense Mutation | CGG,TGG | R15W | XP_016859481.1 |