Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_006295.2 | 3969 | Missense Mutation | CGC,TGC | R1184C | NP_006286.1 |
XM_005249362.2 | 3969 | Missense Mutation | CGC,TGC | R1185C | XP_005249419.1 |
XM_017011246.1 | 3969 | Missense Mutation | CGC,TGC | R602C | XP_016866735.1 |
XM_017011247.1 | 3969 | Missense Mutation | CGC,TGC | R602C | XP_016866736.1 |