Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_017446.3 | 1049 | Intron | NP_059142.2 | ||
NM_080794.3 | 1049 | Missense Mutation | CAT,CGT | H348R | NP_542984.2 |
XM_006724026.3 | 1049 | Missense Mutation | CAT,CGT | H348R | XP_006724089.1 |
XM_011529651.2 | 1049 | Intron | XP_011527953.1 |