| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001146688.1 | 333 | Missense Mutation | CAT,CGT | H92R | NP_001140160.1 |
| NM_018433.5 | 333 | Missense Mutation | CAT,CGT | H92R | NP_060903.2 |
| XM_006712051.3 | 333 | UTR 5 | XP_006712114.1 | ||
| XM_017004493.1 | 333 | Missense Mutation | CAT,CGT | H92R | XP_016859982.1 |
| XM_017004494.1 | 333 | UTR 5 | XP_016859983.1 |