| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001146256.1 | 1455 | Missense Mutation | ACG,ATG | T326M | NP_001139728.1 |
| NM_001146257.1 | 1455 | Intron | NP_001139729.1 | ||
| NM_144969.2 | 1455 | Missense Mutation | ACG,ATG | T335M | NP_659406.1 |
| XM_006724624.3 | 1455 | Missense Mutation | ACG,ATG | T335M | XP_006724687.1 |
| XM_017029296.1 | 1455 | Intron | XP_016884785.1 | ||
| XM_017029297.1 | 1455 | Missense Mutation | ACG,ATG | T186M | XP_016884786.1 |
| XM_017029298.1 | 1455 | Intron | XP_016884787.1 |