Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_020713.2 | 2697 | Missense Mutation | CCT,TCT | P856S | NP_065764.1 |
XM_005260226.3 | 2697 | Missense Mutation | CCT,TCT | P870S | XP_005260283.1 |
XM_011528929.2 | 2697 | Missense Mutation | CCT,TCT | P856S | XP_011527231.1 |
XM_011528930.2 | 2697 | Missense Mutation | CCT,TCT | P837S | XP_011527232.1 |
XM_011528931.2 | 2697 | Missense Mutation | CCT,TCT | P526S | XP_011527233.1 |
XM_011528932.2 | 2697 | Missense Mutation | CCT,TCT | P525S | XP_011527234.1 |
XM_011528933.2 | 2697 | Intron | XP_011527235.1 |