| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001143838.2 | 1499 | Intron | NP_001137310.1 | ||
| NM_001284509.1 | 1499 | Missense Mutation | ATG,GTG | M497V | NP_001271438.1 |
| NM_001284510.1 | 1499 | Missense Mutation | ATG,GTG | M471V | NP_001271439.1 |
| NM_177550.4 | 1499 | Missense Mutation | ATG,GTG | M514V | NP_808218.1 |
| XM_011523795.2 | 1499 | Intron | XP_011522097.1 |