Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_003791.3 | 3379 | Missense Mutation | CAT,CGT | H949R | NP_003782.1 |
XM_017023816.1 | 3379 | Missense Mutation | CAT,CGT | H508R | XP_016879305.1 |
XM_017023817.1 | 3379 | Missense Mutation | CAT,CGT | H453R | XP_016879306.1 |