| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001190997.2 | 1888 | Missense Mutation | CAG,CGG | Q485R | NP_001177926.1 |
| NM_001243392.1 | 1888 | Intron | NP_001230321.1 | ||
| NM_016615.4 | 1888 | Missense Mutation | CAG,CGG | Q577R | NP_057699.2 |
| XM_006719008.3 | 1888 | Missense Mutation | CAG,CGG | Q334R | XP_006719071.1 |
| XM_011521012.2 | 1888 | Missense Mutation | CAG,CGG | Q458R | XP_011519314.1 |
| XM_011521013.1 | 1888 | Missense Mutation | CAG,CGG | Q415R | XP_011519315.1 |
| XM_011521014.1 | 1888 | Missense Mutation | CAG,CGG | Q415R | XP_011519316.1 |
| XM_017019842.1 | 1888 | Missense Mutation | CAG,CGG | Q420R | XP_016875331.1 |
| XM_017019843.1 | 1888 | Missense Mutation | CAG,CGG | Q417R | XP_016875332.1 |
| XM_017019844.1 | 1888 | Intron | XP_016875333.1 | ||
| XM_017019845.1 | 1888 | Missense Mutation | CAG,CGG | Q334R | XP_016875334.1 |
| XM_017019846.1 | 1888 | Intron | XP_016875335.1 | ||
| XM_017019847.1 | 1888 | Intron | XP_016875336.1 |