Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_018946.3 | 185 | Missense Mutation | CCG,CTG | P18L | NP_061819.2 |
XM_011518787.2 | 185 | Intron | XP_011517089.1 | ||
XM_011518788.2 | 185 | Intron | XP_011517090.1 | ||
XM_017014811.1 | 185 | Intron | XP_016870300.1 |