| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001281741.1 | 550 | Intron | NP_001268670.1 | ||
| NM_001281742.1 | 550 | Intron | NP_001268671.1 | ||
| NM_007019.3 | 550 | Intron | NP_008950.1 | ||
| NM_181799.2 | 550 | Intron | NP_861515.1 | ||
| NM_181800.2 | 550 | Intron | NP_861516.1 | ||
| NM_181801.3 | 550 | Missense Mutation | ATG,ATT | M92I | NP_861517.1 |