Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_173489.4 | 5341 | Missense Mutation | CCG,CTG | P1585L | NP_775760.3 |
XM_011513952.1 | 5341 | UTR 3 | XP_011512254.1 | ||
XM_011513953.1 | 5341 | Missense Mutation | CCG,CTG | P1523L | XP_011512255.1 |