| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000582.2 | 579 | Intron | NP_000573.1 | ||
| NM_001040058.1 | 579 | Intron | NP_001035147.1 | ||
| NM_001040060.1 | 579 | Intron | NP_001035149.1 | ||
| NM_001251829.1 | 579 | Intron | NP_001238758.1 | ||
| NM_001251830.1 | 579 | Missense Mutation | GAA,GAC | E9D | NP_001238759.1 |
| XM_017008564.1 | 579 | Missense Mutation | GAA,GAC | E9D | XP_016864053.1 |