Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000076.2 | 207 | Missense Mutation | CGC,CTC | R33L | NP_000067.1 |
NM_001122630.1 | 207 | Missense Mutation | CGC,CTC | R22L | NP_001116102.1 |
NM_001122631.1 | 207 | Missense Mutation | CGC,CTC | R22L | NP_001116103.1 |