| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001017999.2 | 4482 | Intron | NP_001017999.1 | ||
| NM_001018000.3 | 4482 | Intron | NP_001018000.1 | ||
| NM_001018001.2 | 4482 | Intron | NP_001018001.1 | ||
| NM_015209.2 | 4482 | Intron | NP_056024.1 | ||
| NM_201628.2 | 4482 | Missense Mutation | AAT,GAT | N737D | NP_963922.2 |
| XM_005245795.4 | 4482 | Missense Mutation | AAT,GAT | N835D | XP_005245852.1 |
| XM_011541074.2 | 4482 | UTR 3 | XP_011539376.1 | ||
| XM_011541075.2 | 4482 | UTR 3 | XP_011539377.1 | ||
| XM_011541076.2 | 4482 | UTR 3 | XP_011539378.1 | ||
| XM_011541077.2 | 4482 | UTR 3 | XP_011539379.1 | ||
| XM_011541080.2 | 4482 | Intron | XP_011539382.1 | ||
| XM_011541081.2 | 4482 | UTR 3 | XP_011539383.1 | ||
| XM_017000768.1 | 4482 | Intron | XP_016856257.1 | ||
| XM_017000769.1 | 4482 | Intron | XP_016856258.1 | ||
| XM_017000770.1 | 4482 | Intron | XP_016856259.1 | ||
| XM_017000771.1 | 4482 | Intron | XP_016856260.1 | ||
| XM_017000772.1 | 4482 | Intron | XP_016856261.1 |