Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001002814.2 | 3802 | Missense Mutation | CAC,CGC | H1249R | NP_001002814.2 |
NM_025151.4 | 3802 | Missense Mutation | CAC,CGC | H615R | NP_079427.4 |
XM_017013869.1 | 3802 | Intron | XP_016869358.1 |