| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_178858.4 | 359 | Missense Mutation | ATG,CTG | M49L | NP_849189.1 |
| XM_011539261.2 | 359 | Missense Mutation | ATG,CTG | M58L | XP_011537563.1 |
| XM_011539262.2 | 359 | Missense Mutation | ATG,CTG | M49L | XP_011537564.1 |
| XM_011539263.2 | 359 | UTR 5 | XP_011537565.1 | ||
| XM_011539264.2 | 359 | UTR 5 | XP_011537566.1 | ||
| XM_017015663.1 | 359 | Missense Mutation | ATG,CTG | M67L | XP_016871152.1 |