| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_015340.3 | 382 | Missense Mutation | CAA,CGA | Q66R | NP_056155.1 |
| XM_005265006.1 | 382 | Missense Mutation | CAA,CGA | Q66R | XP_005265063.1 |
| XM_011533554.2 | 382 | Missense Mutation | CAA,CGA | Q66R | XP_011531856.1 |
| XM_017006042.1 | 382 | Missense Mutation | CAA,CGA | Q66R | XP_016861531.1 |