| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001145125.1 | 1185 | Intron | NP_001138597.1 | ||
| NM_001291663.1 | 1185 | Intron | NP_001278592.1 | ||
| NM_013446.3 | 1185 | Missense Mutation | ACG,GCG | T391A | NP_038474.2 |
| XM_011515996.1 | 1185 | Missense Mutation | ACG,GCG | T348A | XP_011514298.1 |
| XM_011515997.2 | 1185 | Missense Mutation | ACG,GCG | T327A | XP_011514299.1 |
| XM_011515998.1 | 1185 | Intron | XP_011514300.1 |