Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_025163.3 | 1771 | Missense Mutation | CAT,CGT | H529R | NP_079439.2 |
XM_011513190.1 | 1771 | Missense Mutation | CAT,CGT | H568R | XP_011511492.1 |
XM_011513192.2 | 1771 | Missense Mutation | CAT,CGT | H568R | XP_011511494.1 |
XM_017007240.1 | 1771 | Missense Mutation | CAT,CGT | H594R | XP_016862729.1 |
XM_017007241.1 | 1771 | Missense Mutation | CAT,CGT | H594R | XP_016862730.1 |
XM_017007242.1 | 1771 | Missense Mutation | CAT,CGT | H379R | XP_016862731.1 |
XM_017007243.1 | 1771 | Missense Mutation | CAT,CGT | H379R | XP_016862732.1 |