Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_172089.3 | 1359 | Missense Mutation | CCG,CTG | P284L | NP_742086.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001198622.1 | 1359 | Missense Mutation | CCG,CTG | P177L | NP_001185551.1 |
NM_001198623.1 | 1359 | Missense Mutation | CCG,CTG | P176L | NP_001185552.1 |
NM_001198624.1 | 1359 | Missense Mutation | CCG,CTG | P159L | NP_001185553.1 |
NM_003808.3 | 1359 | Missense Mutation | CCG,CTG | P204L | NP_003799.1 |
NM_172087.2 | 1359 | Missense Mutation | CCG,CTG | P188L | NP_742084.1 |
NM_172088.2 | 1359 | Missense Mutation | CCG,CTG | P204L | NP_742085.1 |