| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001008228.2 | 572 | Missense Mutation | CGG,TGG | R115W | NP_001008229.1 |
| NM_001008229.2 | 572 | Missense Mutation | CGG,TGG | R115W | NP_001008230.1 |
| NM_001170418.1 | 572 | Intron | NP_001163889.1 | ||
| NM_002433.4 | 572 | Missense Mutation | CGG,TGG | R115W | NP_002424.3 |
| NM_206809.3 | 572 | Missense Mutation | CGG,TGG | R115W | NP_996532.2 |
| NM_206810.3 | 572 | Missense Mutation | CGG,TGG | R115W | NP_996533.2 |
| NM_206811.3 | 572 | Missense Mutation | CGG,TGG | R115W | NP_996534.2 |
| NM_206812.3 | 572 | Missense Mutation | CGG,TGG | R115W | NP_996535.2 |
| NM_206814.5 | 572 | Intron | NP_996537.3 | ||
| XM_005249131.3 | 572 | Missense Mutation | CGG,TGG | R115W | XP_005249188.1 |