Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001004326.4 | 358 | Missense Mutation | CGC,TGC | R109C | NP_001004326.4 |
XM_011545043.2 | 358 | Missense Mutation | CGC,TGC | R109C | XP_011543345.1 |
XM_017017774.1 | 358 | Missense Mutation | CGC,TGC | R109C | XP_016873263.1 |
XM_017017775.1 | 358 | Intron | XP_016873264.1 | ||
XM_017017776.1 | 358 | Intron | XP_016873265.1 |