| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001321299.1 | 690 | UTR 5 | NP_001308228.1 | ||
| NM_032387.4 | 690 | Missense Mutation | CGG,TGG | R208W | NP_115763.2 |
| XM_011525135.2 | 690 | Missense Mutation | CGG,TGG | R208W | XP_011523437.1 |
| XM_017024962.1 | 690 | Missense Mutation | CGG,TGG | R208W | XP_016880451.1 |
| XM_017024963.1 | 690 | Missense Mutation | CGG,TGG | R208W | XP_016880452.1 |
| XM_017024964.1 | 690 | Missense Mutation | CGG,TGG | R208W | XP_016880453.1 |
| XM_017024965.1 | 690 | Missense Mutation | CGG,TGG | R208W | XP_016880454.1 |
| XM_017024966.1 | 690 | Intron | XP_016880455.1 |