Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_022468.4 | 413 | Missense Mutation | CAC,CGC | H59R | NP_071913.1 |
XM_011522602.2 | 413 | Intron | XP_011520904.1 | ||
XM_011522604.2 | 413 | Intron | XP_011520906.1 | ||
XM_011522605.2 | 413 | Intron | XP_011520907.1 | ||
XM_017023561.1 | 413 | Missense Mutation | CAC,CGC | H59R | XP_016879050.1 |