Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_007248.3 | 1144 | Intron | NP_009179.2 | ||
NM_016381.5 | 1144 | Missense Mutation | TCG,TTG | S58L | NP_057465.1 |
NM_033629.4 | 1144 | Missense Mutation | TCG,TTG | S3L | NP_338599.1 |