Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_014868.4 | 697 | Missense Mutation | CAC,CGC | H65R | NP_055683.3 |
XM_005254013.2 | 697 | Missense Mutation | CAC,CGC | H15R | XP_005254070.1 |
XM_006719717.2 | 697 | Missense Mutation | CAC,CGC | H65R | XP_006719780.1 |
XM_017020282.1 | 697 | Missense Mutation | CAC,CGC | H15R | XP_016875771.1 |
XM_017020283.1 | 697 | Missense Mutation | CAC,CGC | H65R | XP_016875772.1 |