Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_025216.2 | 453 | Missense Mutation | CGC,TGC | R113C | NP_079492.2 |
XM_011511929.2 | 453 | Missense Mutation | CGC,TGC | R81C | XP_011510231.1 |
XM_011511930.1 | 453 | Missense Mutation | CGC,TGC | R113C | XP_011510232.1 |