Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001146158.1 | 2049 | Missense Mutation | CAC,CGC | H602R | NP_001139630.1 |
NM_006302.2 | 2049 | Missense Mutation | CAC,CGC | H708R | NP_006293.2 |
XM_017004876.1 | 2049 | Missense Mutation | CAC,CGC | H433R | XP_016860365.1 |
XM_017004877.1 | 2049 | Missense Mutation | CAC,CGC | H433R | XP_016860366.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_012477.3 | 2049 | Intron | NP_036609.1 |