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Mutations on the Protein: P12755 From Positions: 0 To 36

6
0
0
6


OMIM Disease: 164780.0005
p.GLY34CYS
N/A
N/A
SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME


OMIM Disease: 164780.0004
p.GLY34SER
N/A
N/A
SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME


OMIM Disease: 164780.0007
p.GLY34VAL
N/A
N/A
SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME


OMIM Disease: 164780.0002
p.LEU32VAL
N/A
N/A
SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME


OMIM Disease: 164780.0009
p.PRO35GLN
N/A
N/A
SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME


OMIM Disease: 164780.0010
p.PRO35SER
N/A
N/A
SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME


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