Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_022104.3 | 325 | Missense Mutation | CCG,CTG | P16L | NP_071387.1 |
XM_011528980.2 | 325 | Missense Mutation | CCG,CTG | P16L | XP_011527282.1 |
XM_011528981.2 | 325 | Missense Mutation | CCG,CTG | P16L | XP_011527283.1 |
XM_017028013.1 | 325 | Missense Mutation | CCG,CTG | P16L | XP_016883502.1 |
XM_017028014.1 | 325 | UTR 5 | XP_016883503.1 |