Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_007332.2 | 3347 | Missense Mutation | ATG,CTG | M1058L | NP_015628.2 |
XM_011517624.2 | 3347 | Missense Mutation | ATG,CTG | M1083L | XP_011515926.1 |
XM_011517625.2 | 3347 | Missense Mutation | ATG,CTG | M1058L | XP_011515927.1 |
XM_017013946.1 | 3347 | Missense Mutation | ATG,CTG | M1058L | XP_016869435.1 |