| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001077494.3 | 3087 | Intron | NP_001070962.1 | ||
| NM_001261403.2 | 3087 | Intron | NP_001248332.1 | ||
| NM_001288724.1 | 3087 | Intron | NP_001275653.1 | ||
| NM_001322934.1 | 3087 | Intron | NP_001309863.1 | ||
| NM_001322935.1 | 3087 | Intron | NP_001309864.1 | ||
| NM_002502.5 | 3087 | Intron | NP_002493.3 | ||
| XM_011539830.2 | 3087 | Intron | XP_011538132.1 | ||
| XM_011539831.2 | 3087 | Intron | XP_011538133.1 | ||
| XM_017016278.1 | 3087 | Intron | XP_016871767.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001270965.1 | 3087 | Missense Mutation | CGG,TGG | R960W | NP_001257894.1 |
| NM_001270966.1 | 3087 | Missense Mutation | CGG,TGG | R581W | NP_001257895.1 |
| NM_002779.4 | 3087 | Missense Mutation | CGG,TGG | R960W | NP_002770.3 |
| XM_011539968.1 | 3087 | Missense Mutation | CGG,TGG | R960W | XP_011538270.1 |
| XM_011539969.2 | 3087 | Missense Mutation | CGG,TGG | R960W | XP_011538271.1 |
| XM_017016433.1 | 3087 | Missense Mutation | CGG,TGG | R960W | XP_016871922.1 |
| XM_017016434.1 | 3087 | Missense Mutation | CGG,TGG | R960W | XP_016871923.1 |