Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001286433.1 | 326 | Intron | NP_001273362.1 | ||
NM_001286435.1 | 326 | Missense Mutation | CGC,TGC | R99C | NP_001273364.1 |
NM_001286436.1 | 326 | Missense Mutation | CGC,TGC | R29C | NP_001273365.1 |
NM_001286438.1 | 326 | Missense Mutation | CGC,TGC | R29C | NP_001273367.1 |
NM_001286439.1 | 326 | Missense Mutation | CGC,TGC | R29C | NP_001273368.1 |
NM_001286440.1 | 326 | Missense Mutation | CGC,TGC | R29C | NP_001273369.1 |
NM_005009.2 | 326 | Missense Mutation | CGC,TGC | R99C | NP_005000.1 |