| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001277081.1 | 1388 | Missense Mutation | CAC,CGC | H186R | NP_001264010.1 |
| NM_001277082.1 | 1388 | Intron | NP_001264011.1 | ||
| NM_017509.3 | 1388 | Missense Mutation | CAC,CGC | H187R | NP_059979.2 |
| XM_006723265.3 | 1388 | Missense Mutation | CAC,CGC | H187R | XP_006723328.1 |
| XM_011527085.2 | 1388 | Missense Mutation | CAC,CGC | H186R | XP_011525387.1 |
| XM_011527087.2 | 1388 | Intron | XP_011525389.1 | ||
| XM_011527088.2 | 1388 | Intron | XP_011525390.1 | ||
| XM_011527089.2 | 1388 | Intron | XP_011525391.1 | ||
| XM_017026943.1 | 1388 | UTR 3 | XP_016882432.1 |