Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001081442.2 | 1574 | Missense Mutation | CGT,TGT | R496C | NP_001074911.1 |
NM_001081443.2 | 1574 | Missense Mutation | CGT,TGT | R396C | NP_001074912.1 |
NM_001304457.1 | 1574 | Missense Mutation | CGT,TGT | R487C | NP_001291386.1 |
NM_006840.4 | 1574 | Missense Mutation | CGT,TGT | R495C | NP_006831.1 |
XM_011526359.2 | 1574 | Missense Mutation | CGT,TGT | R496C | XP_011524661.1 |
XM_011526360.2 | 1574 | Missense Mutation | CGT,TGT | R495C | XP_011524662.1 |
XM_011526361.2 | 1574 | Missense Mutation | CGT,TGT | R479C | XP_011524663.1 |
XM_011526362.2 | 1574 | Missense Mutation | CGT,TGT | R396C | XP_011524664.1 |