Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001145204.2 | 1032 | Intron | NP_001138676.2 | ||
NM_001145205.1 | 1032 | Missense Mutation | ACG,ATG | T196M | NP_001138677.2 |
XM_005255539.3 | 1032 | Intron | XP_005255596.2 | ||
XM_011522642.2 | 1032 | Intron | XP_011520944.1 |