Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001195736.1 | 667 | Missense Mutation | ATC,GTC | I211V | NP_001182665.1 |
NM_001195737.1 | 667 | Intron | NP_001182666.1 | ||
NM_001195738.1 | 667 | Intron | NP_001182667.1 | ||
NM_001195740.1 | 667 | Intron | NP_001182669.1 | ||
NM_001195741.1 | 667 | Intron | NP_001182670.1 | ||
NM_152371.3 | 667 | Missense Mutation | ATC,GTC | I193V | NP_689584.2 |
XM_006710354.3 | 667 | Silent Mutation | TCA,TCG | S199S | XP_006710417.1 |
XM_011540664.1 | 667 | Silent Mutation | TCA,TCG | S217S | XP_011538966.1 |
XM_011540665.1 | 667 | Intron | XP_011538967.1 | ||
XM_011540666.1 | 667 | Intron | XP_011538968.1 |