Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001297598.1 | 1464 | Silent Mutation | CCG,CCT | P472P | NP_001284527.1 |
NM_001297599.1 | 1464 | Silent Mutation | CCG,CCT | P467P | NP_001284528.1 |
NM_152622.4 | 1464 | Silent Mutation | CCG,CCT | P466P | NP_689835.3 |
XM_011543216.1 | 1464 | Silent Mutation | CCG,CCT | P483P | XP_011541518.1 |
XM_011543217.1 | 1464 | Silent Mutation | CCG,CCT | P482P | XP_011541519.1 |
XM_017009149.1 | 1464 | Silent Mutation | CCG,CCT | P291P | XP_016864638.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001171990.2 | 1464 | Intron | NP_001165461.1 | ||
NM_001323018.1 | 1464 | Intron | NP_001309947.1 | ||
NM_001323019.1 | 1464 | Intron | NP_001309948.1 | ||
NM_001323020.1 | 1464 | Intron | NP_001309949.1 | ||
NM_001323022.1 | 1464 | Intron | NP_001309951.1 | ||
NM_153706.3 | 1464 | Intron | NP_714917.2 | ||
XM_005248426.4 | 1464 | Intron | XP_005248483.1 | ||
XM_011543139.2 | 1464 | Intron | XP_011541441.1 | ||
XM_011543140.2 | 1464 | Intron | XP_011541442.1 |