| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001243108.1 | 520 | Missense Mutation | CGG,TGG | R149W | NP_001230037.1 |
| NM_002663.4 | 520 | Missense Mutation | CGG,TGG | R149W | NP_002654.3 |
| XM_005256696.2 | 520 | Intron | XP_005256753.1 | ||
| XM_017024764.1 | 520 | UTR 5 | XP_016880253.1 |