Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001202855.2 | 1567 | Missense Mutation | CAC,CCC | H487P | NP_001189784.1 |
NM_017460.5 | 1567 | Missense Mutation | CAC,CCC | H488P | NP_059488.2 |
XM_017011780.1 | 1567 | Intron | XP_016867269.1 |