Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001294337.1 | 513 | Intron | NP_001281266.1 | ||
NM_001306149.1 | 513 | Missense Mutation | CCT,GCT | P127A | NP_001293078.1 |
NM_001306150.1 | 513 | Missense Mutation | CCT,GCT | P127A | NP_001293079.1 |
NM_178569.3 | 513 | Missense Mutation | CCT,GCT | P127A | NP_848664.1 |
XM_005248256.3 | 513 | Intron | XP_005248313.1 | ||
XM_005248257.3 | 513 | UTR 3 | XP_005248314.1 | ||
XM_011513975.2 | 513 | UTR 3 | XP_011512277.1 | ||
XM_011513977.2 | 513 | Intron | XP_011512279.1 |