Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001205301.1 | 423 | Missense Mutation | CCA,CGA | P26R | NP_001192230.1 |
NM_152403.3 | 423 | Missense Mutation | CCA,CGA | P26R | NP_689616.2 |
NM_182798.2 | 423 | Intron | NP_877950.1 | ||
NM_182801.2 | 423 | Intron | NP_877953.1 |