| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_178026.2 | 1495 | Missense Mutation | GCA,GGA | A658G | NP_821158.2 |
| XM_011528782.2 | 1495 | Missense Mutation | GCA,GGA | A424G | XP_011527084.1 |
| XM_011528783.2 | 1495 | Missense Mutation | GCA,GGA | A375G | XP_011527085.1 |
| XM_017027809.1 | 1495 | UTR 3 | XP_016883298.1 | ||
| XM_017027810.1 | 1495 | Intron | XP_016883299.1 | ||
| XM_017027811.1 | 1495 | Intron | XP_016883300.1 |