| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_005560.4 | 10772 | Missense Mutation | NP_005551.3 | ||
| XM_006723796.3 | 10772 | Missense Mutation | XP_006723859.1 | ||
| XM_006723798.3 | 10772 | Intron | XP_006723861.1 | ||
| XM_011528818.2 | 10772 | Missense Mutation | XP_011527120.1 | ||
| XM_011528819.2 | 10772 | Missense Mutation | XP_011527121.1 |