Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_024512.4 | 1397 | Missense Mutation | CGG,CTG | R335L | NP_078788.2 |
XM_011534110.2 | 1397 | Missense Mutation | CGG,CTG | R335L | XP_011532412.1 |
XM_017007177.1 | 1397 | Intron | XP_016862666.1 |