Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001164189.1 | 1264 | Missense Mutation | CGC,TGC | R362C | NP_001157661.1 |
NM_001164194.1 | 1264 | Missense Mutation | CGC,TGC | R351C | NP_001157666.1 |
NM_005817.4 | 1264 | Missense Mutation | CGC,TGC | R363C | NP_005808.3 |