Yes, but the equilibrium is dynamic and not static. Remember, that there is a tautomerism between the enamines, as well between their chiral forms. The stronger the base, the faster the tautomerism is.
For your own education and for the same steric hindrance reasons, deprotonation of the more-substituted carbon is more convention via formation of the trimethylsilylenol ether, instead of using the enamine (Please,take a look to the literature, when you have time).