Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_138477.2 | 3446 | Missense Mutation | CCG,CTG | P1130L | NP_612486.2 |
XM_005254176.4 | 3446 | Missense Mutation | CCG,CTG | P1131L | XP_005254233.1 |
XM_011521270.2 | 3446 | Missense Mutation | CCG,CTG | P1139L | XP_011519572.1 |
XM_011521271.2 | 3446 | Missense Mutation | CCG,CTG | P1138L | XP_011519573.1 |
XM_011521274.2 | 3446 | Missense Mutation | CCG,CTG | P794L | XP_011519576.1 |