Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_032444.2 | 5313 | Missense Mutation | CGC,TGC | R1761C | NP_115820.2 |
XM_011522715.2 | 5313 | Missense Mutation | CGC,TGC | R1760C | XP_011521017.1 |
XM_017023775.1 | 5313 | Missense Mutation | CGC,TGC | R1487C | XP_016879264.1 |