| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_004565.2 | 47 | Missense Mutation | CAG,CTG | Q9L | NP_004556.1 |
| XM_005263470.4 | 47 | Intron | XP_005263527.1 | ||
| XM_011541577.2 | 47 | Intron | XP_011539879.1 | ||
| XM_011541578.2 | 47 | Intron | XP_011539880.1 | ||
| XM_011541579.2 | 47 | Intron | XP_011539881.1 | ||
| XM_011541580.1 | 47 | Missense Mutation | CAG,CTG | Q9L | XP_011539882.1 |