| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001276700.1 | 389 | Missense Mutation | ATG,GTG | M62V | NP_001263629.1 |
| NM_138329.2 | 389 | Missense Mutation | ATG,GTG | M62V | NP_612202.2 |
| XM_011519931.1 | 389 | Missense Mutation | ATG,GTG | M62V | XP_011518233.1 |
| XM_017017252.1 | 389 | Missense Mutation | ATG,GTG | M62V | XP_016872741.1 |
| XM_017017253.1 | 389 | Intron | XP_016872742.1 |