| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001031666.1 | 47 | Intron | NP_001026836.1 | ||
| NM_001031809.1 | 47 | Intron | NP_001026979.1 | ||
| NM_006138.4 | 47 | Missense Mutation | AAT,TAT | N58Y | NP_006129.4 |
| XM_011545363.2 | 47 | UTR 5 | XP_011543665.1 |