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Results 11 - 15 of 15

EC Number	Protein Variants	Commentary	Reference
1.11.1.8	P499L	natural missense mutation, mutant shows higher Km values and lower reaction efficiencies thna wild-type	743286
1.11.1.8	Q446H	the mutation is associated with the occurrence of congenital hypothyroidism	695403
1.11.1.8	R479C	a novel hypothyroid dwarfism due to the missense mutation R479C of the thyroid peroxidase gene in the mouse	676000
1.11.1.8	W527C	the mutation is associated with the occurrence of congenital hypothyroidism	695403
1.11.1.8	W873X	the mutation is associated with the occurrence of congenital hypothyroidism	695403

Results 11 - 15 of 15

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Release 2023.1 (January 2023)