Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001317962.1 | 239 | Missense Mutation | CCA,CGA | P10R | NP_001304891.1 |
NM_001317963.1 | 239 | UTR 5 | NP_001304892.1 | ||
NM_007062.2 | 239 | Missense Mutation | CCA,CGA | P72R | NP_008993.1 |