Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001278717.1 | 357 | Missense Mutation | CGC,TGC | R90C | NP_001265646.1 |
NM_001278718.1 | 357 | Missense Mutation | CGC,TGC | R90C | NP_001265647.1 |
NM_005031.4 | 357 | Missense Mutation | CGC,TGC | R90C | NP_005022.2 |
NM_021902.3 | 357 | Missense Mutation | CGC,TGC | R90C | NP_068702.1 |
XM_017026874.1 | 357 | Missense Mutation | CGC,TGC | R90C | XP_016882363.1 |
XM_017026875.1 | 357 | Missense Mutation | CGC,TGC | R108C | XP_016882364.1 |
XM_017026876.1 | 357 | Missense Mutation | CGC,TGC | R108C | XP_016882365.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_022006.1 | 357 | Intron | NP_071289.1 |