Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_030939.4 | 1335 | Missense Mutation | CGC,TGC | R163C | NP_112201.1 |
XM_005249433.3 | 1335 | Intron | XP_005249490.1 | ||
XM_011514928.2 | 1335 | Missense Mutation | CGC,TGC | R134C | XP_011513230.1 |