| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001256030.1 | 687 | Missense Mutation | CAG,CAT | Q177H | NP_001242959.1 |
| NM_001778.3 | 687 | Missense Mutation | CAG,CAT | Q177H | NP_001769.2 |
| XM_005245625.1 | 687 | Intron | XP_005245682.1 | ||
| XM_011510171.1 | 687 | Missense Mutation | CAG,CAT | Q145H | XP_011508473.1 |
| XM_017002867.1 | 687 | Missense Mutation | CAG,CAT | Q76H | XP_016858356.1 |