| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001005376.2 | 718 | Missense Mutation | ACC,GCC | T224A | NP_001005376.1 |
| NM_001005377.2 | 718 | Missense Mutation | ACC,GCC | T179A | NP_001005377.1 |
| NM_001301037.1 | 718 | Intron | NP_001287966.1 | ||
| NM_002659.3 | 718 | Missense Mutation | ACC,GCC | T224A | NP_002650.1 |
| XM_005258990.4 | 718 | Missense Mutation | ACC,GCC | T224A | XP_005259047.1 |
| XM_011527027.2 | 718 | Missense Mutation | ACC,GCC | T176A | XP_011525329.1 |
| XM_011527028.2 | 718 | Silent Mutation | GCA,GCG | A230A | XP_011525330.1 |
| XM_011527029.1 | 718 | Silent Mutation | GCA,GCG | A230A | XP_011525331.1 |
| XM_011527030.2 | 718 | Intron | XP_011525332.1 | ||
| XM_011527031.2 | 718 | Intron | XP_011525333.1 | ||
| XM_017026872.1 | 718 | Missense Mutation | ACC,GCC | T219A | XP_016882361.1 |
| XM_017026873.1 | 718 | Missense Mutation | ACC,GCC | T100A | XP_016882362.1 |