Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001006941.2 | 887 | Missense Mutation | TCC,TGC | S276C | NP_001006942.1 |
NM_005787.5 | 887 | Missense Mutation | TCC,TGC | S324C | NP_005778.1 |
XM_011512322.1 | 887 | Missense Mutation | TCC,TGC | S291C | XP_011510624.1 |
XM_011512323.2 | 887 | Missense Mutation | TCC,TGC | S284C | XP_011510625.1 |