| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001277090.1 | 1329 | Missense Mutation | ACG,ATG | T384M | NP_001264019.1 |
| NM_001277091.1 | 1329 | Missense Mutation | ACG,ATG | T384M | NP_001264020.1 |
| NM_001277092.1 | 1329 | Missense Mutation | ACG,ATG | T384M | NP_001264021.1 |
| NM_001277093.1 | 1329 | Intron | NP_001264022.1 | ||
| XM_011526567.2 | 1329 | Missense Mutation | ACG,ATG | T384M | XP_011524869.1 |
| XM_011526568.2 | 1329 | Missense Mutation | ACG,ATG | T375M | XP_011524870.1 |
| XM_017026401.1 | 1329 | Missense Mutation | ACG,ATG | T384M | XP_016881890.1 |