| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001033024.1 | 557 | Intron | NP_001028196.1 | ||
| NM_001257990.1 | 557 | UTR 5 | NP_001244919.1 | ||
| NM_012179.3 | 557 | Missense Mutation | CAT,GAT | H92D | NP_036311.3 |
| XM_011530106.1 | 557 | Intron | XP_011528408.1 |