| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001270873.1 | 393 | Missense Mutation | ATG,GTG | M47V | NP_001257802.1 |
| NM_033223.4 | 393 | Missense Mutation | ATG,GTG | M47V | NP_150092.2 |
| XM_011521430.2 | 393 | Missense Mutation | ATG,GTG | M47V | XP_011519732.1 |
| XM_011521431.2 | 393 | Intron | XP_011519733.1 | ||
| XM_017022058.1 | 393 | Intron | XP_016877547.1 | ||
| XM_017022059.1 | 393 | Intron | XP_016877548.1 | ||
| XM_017022060.1 | 393 | Intron | XP_016877549.1 |