Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000203.4 | 252 | Missense Mutation | CCG,CTG | P55L | NP_000194.2 |
XM_011513461.2 | 252 | Intron | XP_011511763.1 | ||
XM_017008163.1 | 252 | UTR 5 | XP_016863652.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_022042.3 | 252 | UTR 3 | NP_071325.2 | ||
NM_134425.2 | 252 | Intron | NP_602297.1 | ||
NM_213613.3 | 252 | UTR 3 | NP_998778.1 |