Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001319243.1 | 611 | Missense Mutation | CCG,CTG | P343L | NP_001306172.1 |
NM_001319244.1 | 611 | Missense Mutation | CCG,CTG | P192L | NP_001306173.1 |
NM_001319302.1 | 611 | Missense Mutation | CCG,CTG | P192L | NP_001306231.1 |
NM_178314.4 | 611 | Missense Mutation | CCG,CTG | P343L | NP_847884.2 |
XM_006719372.2 | 611 | Missense Mutation | CCG,CTG | P343L | XP_006719435.1 |
XM_006719373.3 | 611 | Missense Mutation | CCG,CTG | P192L | XP_006719436.1 |
XM_011538282.2 | 611 | Missense Mutation | CCG,CTG | P275L | XP_011536584.1 |
XM_011538284.2 | 611 | Missense Mutation | CCG,CTG | P189L | XP_011536586.1 |
XM_011538285.2 | 611 | Missense Mutation | CCG,CTG | P189L | XP_011536587.1 |