Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_014398.3 | 1354 | Missense Mutation | TCG,TTG | S377L | NP_055213.2 |
XM_005247360.4 | 1354 | Intron | XP_005247417.1 | ||
XM_006713586.3 | 1354 | Intron | XP_006713649.1 | ||
XM_011512688.1 | 1354 | Intron | XP_011510990.1 |