| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_025009.4 | 333 | Missense Mutation | CAC,CGC | H22R | NP_079285.2 |
| XM_005265788.3 | 333 | UTR 5 | XP_005265845.1 | ||
| XM_006714055.2 | 333 | Missense Mutation | CAC,CGC | H22R | XP_006714118.1 |
| XM_011534412.2 | 333 | Intron | XP_011532714.1 |