Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001168278.1 | 1270 | Missense Mutation | CGT,TGT | R356C | NP_001161750.1 |
NM_001168280.1 | 1270 | Missense Mutation | CGT,TGT | R356C | NP_001161752.1 |
NM_015472.4 | 1270 | Missense Mutation | CGT,TGT | R356C | NP_056287.1 |
XM_017006121.1 | 1270 | Missense Mutation | CGT,TGT | R356C | XP_016861610.1 |
XM_017006122.1 | 1270 | Missense Mutation | CGT,TGT | R356C | XP_016861611.1 |