Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001300861.1 | 649 | Intron | NP_001287790.1 | ||
NM_020470.2 | 649 | Missense Mutation | TCC,TGC | S164C | NP_065203.2 |
XM_005273720.3 | 649 | Missense Mutation | TCC,TGC | S164C | XP_005273777.1 |
XM_017017139.1 | 649 | Missense Mutation | TCC,TGC | S176C | XP_016872628.1 |
XM_017017140.1 | 649 | Missense Mutation | TCC,TGC | S176C | XP_016872629.1 |
XM_017017141.1 | 649 | Intron | XP_016872630.1 |