Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001039140.2 | 1080 | Missense Mutation | CGC,TGC | R158C | NP_001034229.1 |
NM_001258429.1 | 1080 | Missense Mutation | CGC,TGC | R133C | NP_001245358.1 |
NM_001258430.1 | 1080 | Missense Mutation | CGC,TGC | R133C | NP_001245359.1 |
XM_011529266.2 | 1080 | Intron | XP_011527568.1 |