Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001145391.1 | 690 | Missense Mutation | CGA,GGA | R195G | NP_001138863.1 |
NM_017897.2 | 690 | Missense Mutation | CGA,GGA | R195G | NP_060367.1 |
XM_006713216.3 | 690 | Missense Mutation | CGA,GGA | R195G | XP_006713279.1 |
XM_006713217.3 | 690 | Intron | XP_006713280.1 | ||
XM_017006713.1 | 690 | Missense Mutation | CGA,GGA | R195G | XP_016862202.1 |
XM_017006714.1 | 690 | Intron | XP_016862203.1 |