Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001267608.1 | 2269 | Missense Mutation | CGC,TGC | R537C | NP_001254537.1 |
NM_006589.2 | 2269 | Missense Mutation | CGC,TGC | R555C | NP_006580.2 |
NM_198264.1 | 2269 | Missense Mutation | CGC,TGC | R459C | NP_937995.1 |
XM_005244845.1 | 2269 | Missense Mutation | CGC,TGC | R556C | XP_005244902.1 |