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Mutations on the Protein: P08865 From Positions: 44 To 59

2
0
0
2


OMIM Disease: 150370.0007
p.LEU58PHE
N/A
N/A
ASPLENIA, ISOLATED CONGENITAL


OMIM Disease: 150370.0006
p.THR54ASN
N/A
N/A
ASPLENIA, ISOLATED CONGENITAL






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