| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001009936.2 | 1589 | Intron | NP_001009936.1 | ||
| NM_001286840.1 | 1589 | Missense Mutation | CGG,TGG | R508W | NP_001273769.1 |
| NM_001286842.1 | 1589 | Missense Mutation | CGG,TGG | R280W | NP_001273771.1 |
| NM_001286843.1 | 1589 | Intron | NP_001273772.1 | ||
| NM_015651.2 | 1589 | Missense Mutation | CGG,TGG | R489W | NP_056466.1 |
| XM_005251906.2 | 1589 | Missense Mutation | CGG,TGG | R489W | XP_005251963.1 |
| XM_011518509.2 | 1589 | Missense Mutation | CGG,TGG | R489W | XP_011516811.1 |
| XM_011518511.2 | 1589 | UTR 3 | XP_011516813.1 | ||
| XM_011518515.2 | 1589 | Intron | XP_011516817.1 | ||
| XM_011518516.2 | 1589 | Intron | XP_011516818.1 | ||
| XM_017014612.1 | 1589 | Missense Mutation | CGG,TGG | R489W | XP_016870101.1 |
| XM_017014613.1 | 1589 | Intron | XP_016870102.1 |