| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_021232.1 | 1391 | Missense Mutation | CGG,TGG | R506W | NP_067055.1 |
| XM_017027084.1 | 1391 | Missense Mutation | CGG,TGG | R430W | XP_016882573.1 |
| XM_017027085.1 | 1391 | UTR 3 | XP_016882574.1 |