Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001168388.2 | 638 | Missense Mutation | CAC,CGC | H131R | NP_001161860.1 |
NM_001168389.2 | 638 | Missense Mutation | CAC,CGC | H136R | NP_001161861.2 |
NM_006079.4 | 638 | Missense Mutation | CAC,CGC | H131R | NP_006070.2 |