Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001142797.1 | 846 | Missense Mutation | CCG,CTG | P273L | NP_001136269.1 |
NM_001504.1 | 846 | Missense Mutation | CCG,CTG | P226L | NP_001495.1 |
XM_005262256.3 | 846 | Missense Mutation | CCG,CTG | P236L | XP_005262313.1 |
XM_005262257.3 | 846 | Intron | XP_005262314.1 | ||
XM_017029435.1 | 846 | Missense Mutation | CCG,CTG | P273L | XP_016884924.1 |
XM_017029436.1 | 846 | Intron | XP_016884925.1 |