Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001168271.1 | 2731 | Missense Mutation | CGC,TGC | R753C | NP_001161743.1 |
NM_153002.2 | 2731 | Missense Mutation | CGC,TGC | R757C | NP_694547.2 |
XM_005247165.2 | 2731 | Missense Mutation | CGC,TGC | R757C | XP_005247222.1 |
XM_011512484.2 | 2731 | Missense Mutation | CGC,TGC | R676C | XP_011510786.1 |
XM_011512487.1 | 2731 | Missense Mutation | CGC,TGC | R676C | XP_011510789.1 |
XM_011512488.2 | 2731 | Missense Mutation | CGC,TGC | R371C | XP_011510790.1 |
XM_017005795.1 | 2731 | Missense Mutation | CGC,TGC | R757C | XP_016861284.1 |
XM_017005796.1 | 2731 | Missense Mutation | CGC,TGC | R757C | XP_016861285.1 |
XM_017005797.1 | 2731 | Missense Mutation | CGC,TGC | R753C | XP_016861286.1 |