Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001316964.1 | 1100 | Intron | NP_001303893.1 | ||
NM_001316965.1 | 1100 | Silent Mutation | CGC,CGG | R165R | NP_001303894.1 |
NM_025232.3 | 1100 | Missense Mutation | CCA,GCA | P211A | NP_079508.2 |