| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001196.3 | 589 | Missense Mutation | CAA,CAC | Q162H | NP_001187.1 |
| NM_001244567.1 | 589 | Missense Mutation | CAA,CAC | Q162H | NP_001231496.1 |
| NM_001244569.1 | 589 | Missense Mutation | CAA,CAC | Q66H | NP_001231498.1 |
| NM_001244570.1 | 589 | Missense Mutation | CAA,CAC | Q66H | NP_001231499.1 |
| NM_001244572.1 | 589 | Missense Mutation | CAA,CAC | Q66H | NP_001231501.1 |
| NM_197966.2 | 589 | Missense Mutation | CAA,CAC | Q208H | NP_932070.1 |
| NM_197967.2 | 589 | Missense Mutation | CAA,CAC | Q66H | NP_932071.1 |
| XM_017028906.1 | 589 | Missense Mutation | CAA,CAC | Q162H | XP_016884395.1 |