Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001001790.2 | 241 | Intron | NP_001001790.1 | ||
NM_001134484.1 | 241 | Missense Mutation | CCG,CTG | P45L | NP_001127956.1 |
NM_001134485.1 | 241 | Missense Mutation | CCG,CTG | P45L | NP_001127957.1 |