| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001491.2 | 634 | Intron | NP_001482.1 | ||
| NM_145649.4 | 634 | Missense Mutation | CGG,TGG | R29W | NP_663624.1 |
| NM_145655.3 | 634 | Intron | NP_663630.2 | ||
| XM_005248997.3 | 634 | Intron | XP_005249054.1 | ||
| XM_005248999.2 | 634 | Intron | XP_005249056.1 | ||
| XM_006715052.3 | 634 | Missense Mutation | CGG,TGG | R29W | XP_006715115.1 |
| XM_011514466.2 | 634 | Intron | XP_011512768.1 | ||
| XM_011514468.2 | 634 | Missense Mutation | CGG,TGG | R29W | XP_011512770.1 |
| XM_017010732.1 | 634 | Missense Mutation | CGG,TGG | R29W | XP_016866221.1 |