Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001308277.1 | 587 | Missense Mutation | CAC,CGC | H93R | NP_001295206.1 |
NM_018381.3 | 587 | Missense Mutation | CAC,CGC | H93R | NP_060851.2 |
XM_011528121.1 | 587 | Missense Mutation | CAC,CGC | H54R | XP_011526423.1 |
XM_011528122.1 | 587 | Intron | XP_011526424.1 | ||
XM_017026934.1 | 587 | Missense Mutation | CAC,CGC | H42R | XP_016882423.1 |