Oncogenic mutations can destabilize signaling proteins, resulting in increased or unregulated activity. Thus, there is considerable interest in mapping the relationship between mutations and the stability of signaling proteins, to better understand the consequences of oncogenic mutations and potentially inform the development of new therapeutics. Here, we develop a tool to study protein‐kinase stability in live mammalian cells and the effects of the HSP90 chaperone system on the stability of these kinases. We determine the expression levels of protein kinases by monitoring the fluorescence of fluorescent proteins fused to those kinases, normalized to that of co‐expressed reference fluorescent proteins. We used this tool to study the dependence of Src‐ and Raf‐family kinases on the HSP90 system. We demonstrate that this sensor reports on destabilization induced by oncogenic mutations in these kinases. We also show that Src‐homology 2 and Src‐homology 3 domains, which are required for autoinhibition of Src‐family kinases, stabilize these kinase domains in the cell. Our expression‐calibrated sensor enables the facile characterization of the effects of mutations and small‐molecule drugs on protein‐kinase stability.