Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_003659.3 | 261 | Missense Mutation | ACG,GCG | T72A | NP_003650.1 |
XM_011512041.2 | 261 | Intron | XP_011510343.1 | ||
XM_011512042.1 | 261 | Intron | XP_011510344.1 | ||
XM_011512043.2 | 261 | Intron | XP_011510345.1 |