| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001300883.2 | 1627 | Missense Mutation | CAC,CGC | H432R | NP_001287812.1 |
| NM_001318055.1 | 1627 | Intron | NP_001304984.1 | ||
| NM_001318056.1 | 1627 | Intron | NP_001304985.1 | ||
| NM_024106.2 | 1627 | Intron | NP_077011.1 | ||
| XM_017027293.1 | 1627 | Missense Mutation | CAC,CGC | H432R | XP_016882782.1 |
| XM_017027294.1 | 1627 | Missense Mutation | CAC,CGC | H228R | XP_016882783.1 |