Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001146221.1 | 899 | Missense Mutation | TCT,TGT | S300C | NP_001139693.1 |
XM_006719024.3 | 899 | Missense Mutation | TCT,TGT | S255C | XP_006719087.1 |
XM_011520542.2 | 899 | Missense Mutation | TCT,TGT | S273C | XP_011518844.1 |