Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_198488.3 | 4203 | Missense Mutation | CGC,TGC | R980C | NP_940890.3 |
XM_005250887.3 | 4203 | Missense Mutation | CGC,TGC | R999C | XP_005250944.1 |
XM_005250888.3 | 4203 | Missense Mutation | CGC,TGC | R986C | XP_005250945.1 |
XM_005250889.3 | 4203 | Missense Mutation | CGC,TGC | R980C | XP_005250946.1 |
XM_011516980.2 | 4203 | Missense Mutation | CGC,TGC | R1181C | XP_011515282.2 |
XM_011516981.2 | 4203 | Missense Mutation | CGC,TGC | R1036C | XP_011515283.1 |