| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_020857.2 | 526 | Missense Mutation | CAC,CGC | H56R | NP_065908.1 |
| XM_011521843.2 | 526 | Intron | XP_011520145.1 | ||
| XM_011521844.2 | 526 | UTR 5 | XP_011520146.1 | ||
| XM_017022447.1 | 526 | UTR 5 | XP_016877936.1 |