Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_004750.4 | 1533 | Silent Mutation | CCC,CCT | P420P | NP_004741.1 |
XM_011528422.2 | 1533 | Intron | XP_011526724.1 | ||
XM_011528423.2 | 1533 | UTR 3 | XP_011526725.1 | ||
XM_011528424.2 | 1533 | Missense Mutation | CCG,CTG | P400L | XP_011526726.1 |