Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_033396.2 | 4955 | Missense Mutation | TCG,TTG | S1597L | NP_203754.2 |
XM_006718725.3 | 4955 | Missense Mutation | TCG,TTG | S1597L | XP_006718788.1 |
XM_011545325.2 | 4955 | Intron | XP_011543627.1 |