| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001293186.1 | 691 | Missense Mutation | CAA,CAC | Q166H | NP_001280115.1 |
| NM_001293187.1 | 691 | Missense Mutation | CAA,CAC | Q166H | NP_001280116.1 |
| NM_014168.3 | 691 | Missense Mutation | CAA,CAC | Q166H | NP_054887.2 |
| XM_011511023.1 | 691 | Intron | XP_011509325.1 |