Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001160045.1 | 383 | Intron | NP_001153517.1 | ||
NM_001167609.1 | 383 | Missense Mutation | CCG,CGG | P20R | NP_001161081.1 |
NM_005269.2 | 383 | Missense Mutation | CCG,CGG | P20R | NP_005260.1 |
XM_011538189.2 | 383 | Missense Mutation | CCG,CGG | P20R | XP_011536491.1 |
XM_011538190.1 | 383 | Missense Mutation | CCG,CGG | P20R | XP_011536492.1 |