Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001385.2 | 1572 | Missense Mutation | CAT,CGT | H490R | NP_001376.1 |
XM_005250818.3 | 1572 | Missense Mutation | CAT,CGT | H526R | XP_005250875.1 |
XM_006716518.3 | 1572 | Missense Mutation | CAT,CGT | H473R | XP_006716581.1 |
XM_011516903.2 | 1572 | Intron | XP_011515205.1 | ||
XM_017013167.1 | 1572 | Intron | XP_016868656.1 |