| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001289973.1 | 2549 | Missense Mutation | ACG,ATG | T497M | NP_001276902.1 |
| NM_207411.4 | 2549 | Missense Mutation | ACG,ATG | T660M | NP_997294.3 |
| XM_011534750.2 | 2549 | Missense Mutation | ACG,ATG | T390M | XP_011533052.1 |
| XM_017013401.1 | 2549 | Missense Mutation | ACG,ATG | T662M | XP_016868890.1 |
| XM_017013402.1 | 2549 | Missense Mutation | ACG,ATG | T592M | XP_016868891.1 |