Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001282601.1 | 696 | Missense Mutation | CCT,CTT | P96L | NP_001269530.1 |
NM_001282602.1 | 696 | Intron | NP_001269531.1 | ||
NM_001282603.1 | 696 | Missense Mutation | CCT,CTT | P63L | NP_001269532.1 |
NM_001282604.1 | 696 | Missense Mutation | CCT,CTT | P100L | NP_001269533.1 |
NM_001282605.1 | 696 | Intron | NP_001269534.1 | ||
NM_006601.6 | 696 | Missense Mutation | CCT,CTT | P96L | NP_006592.3 |
XM_005268576.4 | 696 | Missense Mutation | CCT,CTT | P100L | XP_005268633.1 |
XM_006719199.2 | 696 | Intron | XP_006719262.1 | ||
XM_011537773.2 | 696 | Intron | XP_011536075.1 | ||
XM_011537774.2 | 696 | Missense Mutation | CCT,CTT | P100L | XP_011536076.1 |
XM_017018716.1 | 696 | Missense Mutation | CCT,CTT | P100L | XP_016874205.1 |