Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001142547.1 | 907 | Missense Mutation | CGC,TGC | R334C | NP_001136019.1 |
NM_173659.3 | 907 | Missense Mutation | CGC,TGC | R349C | NP_775930.2 |
XM_011533627.2 | 907 | UTR 3 | XP_011531929.1 |