Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001029871.3 | 548 | Missense Mutation | CGC,TGC | R212C | NP_001025042.2 |
NM_001040007.2 | 548 | Missense Mutation | CGC,TGC | R150C | NP_001035096.1 |
XM_017027839.1 | 548 | Intron | XP_016883328.1 |