Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_004279.2 | 390 | Missense Mutation | CCG,CTG | P119L | NP_004270.2 |
XM_005250717.3 | 390 | Missense Mutation | CCG,CTG | P119L | XP_005250774.1 |
XM_006716181.3 | 390 | Missense Mutation | CCG,CTG | P119L | XP_006716244.1 |