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Mutations on the Protein: P51798 From Positions: 725 To 765

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4
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1








Swiss-Prot Disease: VAR_017838
p.ARG762GLN
N/A
N/A
Osteopetrosis, autosomal recessive 4 (OPTB4)


Swiss-Prot Disease: VAR_064647
p.ARG762TRP
N/A
N/A
Osteopetrosis, autosomal recessive 4 (OPTB4)


Swiss-Prot Disease: VAR_064646
p.PHE758LEU
N/A
N/A
Osteopetrosis, autosomal dominant 2 (OPTA2)


Swiss-Prot Disease: VAR_021007
p.SER744PHE
N/A
N/A
Osteopetrosis, autosomal recessive 4 (OPTB4)


OMIM Disease: 602727.0002
p.ARG762GLN
N/A
N/A
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 4






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