Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001204078.1 | 293 | Intron | NP_001191007.1 | ||
NM_130463.3 | 293 | Missense Mutation | CAC,CGC | H53R | NP_569730.1 |
NM_138282.2 | 293 | Missense Mutation | CAC,CGC | H12R | NP_612139.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001144961.1 | 293 | Intron | NP_001138433.1 | ||
NM_001144962.1 | 293 | Intron | NP_001138434.1 | ||
NM_001144963.1 | 293 | Intron | NP_001138435.1 | ||
NM_005007.3 | 293 | Intron | NP_004998.3 |