Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_175734.4 | 452 | Missense Mutation | CGC,TGC | R127C | NP_783861.3 |
XM_006721471.3 | 452 | Missense Mutation | CGC,TGC | R30C | XP_006721534.1 |
XM_011523722.2 | 452 | UTR 5 | XP_011522024.1 |