Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001135219.1 | 2249 | Missense Mutation | CGC,TGC | R386C | NP_001128691.1 |
NM_173492.1 | 2249 | Missense Mutation | CGC,TGC | R183C | NP_775763.1 |
XM_017014279.1 | 2249 | UTR 3 | XP_016869768.1 |