Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_016565.2 | 513 | Missense Mutation | CAC,CGC | H31R | NP_057649.2 |
XM_017017883.1 | 513 | Missense Mutation | CAC,CGC | H40R | XP_016873372.1 |
XM_017017884.1 | 513 | Missense Mutation | CAC,CGC | H31R | XP_016873373.1 |