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Mutations on the Protein: NP_054698 From Positions: 43 To 57

3
0
0
3





OMIM Disease: 167415.0005
p.CYS57TYR
N/A
N/A
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2


OMIM Disease: 167415.0006
p.SER54GLY
N/A
N/A
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2


OMIM Disease: 167415.0008
p.SER48PHE
N/A
N/A
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2






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