| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001040697.2 | 3112 | Missense Mutation | ATG,GTG | M397V | NP_001035787.1 |
| NM_001261382.1 | 3112 | Missense Mutation | ATG,GTG | M375V | NP_001248311.1 |
| NM_001261383.1 | 3112 | Intron | NP_001248312.1 | ||
| NM_001261384.1 | 3112 | Missense Mutation | ATG,GTG | M267V | NP_001248313.1 |
| NM_001261385.1 | 3112 | Intron | NP_001248314.1 | ||
| NM_001261386.1 | 3112 | Intron | NP_001248315.1 | ||
| NM_001297771.1 | 3112 | Intron | NP_001284700.1 | ||
| NM_018314.4 | 3112 | Intron | NP_060784.3 | ||
| XM_006718255.2 | 3112 | Missense Mutation | ATG,GTG | M174V | XP_006718318.1 |
| XM_011520201.2 | 3112 | Missense Mutation | ATG,GTG | M174V | XP_011518503.1 |
| XM_017017985.1 | 3112 | Missense Mutation | ATG,GTG | M267V | XP_016873474.1 |
| XM_017017986.1 | 3112 | Intron | XP_016873475.1 |