Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001171940.1 | 693 | Intron | NP_001165411.2 | ||
NM_001171941.2 | 693 | Missense Mutation | CAC,CGC | H134R | NP_001165412.1 |
NM_153756.2 | 693 | Missense Mutation | CAC,CGC | H209R | NP_715637.2 |