Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_198478.3 | 4037 | Missense Mutation | CGC,TGC | R687C | NP_940880.3 |
XM_011526799.2 | 4037 | Missense Mutation | CGC,TGC | R714C | XP_011525101.1 |
XM_011526802.2 | 4037 | Missense Mutation | CGC,TGC | R687C | XP_011525104.1 |
XM_011526804.2 | 4037 | Missense Mutation | CGC,TGC | R568C | XP_011525106.1 |
XM_011526805.2 | 4037 | Missense Mutation | CGC,TGC | R512C | XP_011525107.1 |