Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_030923.4 | 1020 | Missense Mutation | CAT,CGT | H283R | NP_112185.1 |
XM_011511950.2 | 1020 | Missense Mutation | CAT,CGT | H172R | XP_011510252.1 |
XM_017005060.1 | 1020 | Intron | XP_016860549.1 | ||
XM_017005061.1 | 1020 | Missense Mutation | CAT,CGT | H172R | XP_016860550.1 |
XM_017005062.1 | 1020 | Intron | XP_016860551.1 |