Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001308053.1 | 669 | Missense Mutation | ACC,GCC | T100A | NP_001294982.1 |
NM_014353.4 | 669 | Missense Mutation | ACC,GCC | T166A | NP_055168.2 |
XM_011522448.1 | 669 | Missense Mutation | ACC,GCC | T166A | XP_011520750.1 |
XM_011522450.2 | 669 | Missense Mutation | ACC,GCC | T50A | XP_011520752.1 |