| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001032998.1 | 166 | Missense Mutation | ACG,ATG | T25M | NP_001028170.1 |
| NM_001199241.1 | 166 | Missense Mutation | ACG,ATG | T25M | NP_001186170.1 |
| NM_003937.2 | 166 | Missense Mutation | ACG,ATG | T25M | NP_003928.1 |
| XM_011512102.2 | 166 | Intron | XP_011510404.1 | ||
| XM_017005217.1 | 166 | Missense Mutation | ACG,ATG | T25M | XP_016860706.1 |