Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001008777.2 | 1388 | Missense Mutation | CAT,CGT | H429R | NP_001008777.2 |
XM_011524865.2 | 1388 | Missense Mutation | CAT,CGT | H403R | XP_011523167.1 |
XM_011524866.2 | 1388 | Missense Mutation | CAT,CGT | H372R | XP_011523168.1 |
XM_011524867.2 | 1388 | Intron | XP_011523169.1 |