| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_004823.1 | 1168 | Missense Mutation | CGG,TGG | R166W | NP_004814.1 |
| XM_011527526.1 | 1168 | Missense Mutation | CGG,TGG | R32W | XP_011525828.1 |
| XM_011527527.1 | 1168 | Intron | XP_011525829.1 | ||
| XM_017027506.1 | 1168 | Intron | XP_016882995.1 |