| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| XM_017000534.1 | 2982 | Missense Mutation | CAC,CAG | H965Q | XP_016856023.1 |
| XM_017000535.1 | 2982 | Missense Mutation | CAC,CAG | H957Q | XP_016856024.1 |
| XM_017000536.1 | 2982 | Missense Mutation | CAC,CAG | H914Q | XP_016856025.1 |
| XM_017000537.1 | 2982 | Intron | XP_016856026.1 |