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Mutations on the Protein: NP_001159434 From Positions: 472 To 511

2
0
0
2




OMIM Disease: 605367.0002
p.ALA501THR
N/A
N/A
PROSTATE CANCER, HEREDITARY, 2


OMIM Disease: 605367.0007
p.THR480ILE
N/A
N/A
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 17






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