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Mutations on the Protein: P68133 From Positions: 207 To 226

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3
0
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Swiss-Prot Disease: VAR_062458
p.GLU226GLN
N/A
N/A
Nemaline myopathy 3 (NEM3)


Swiss-Prot Disease: VAR_062457
p.GLU226GLY
N/A
N/A
Nemaline myopathy 3 (NEM3)


Swiss-Prot Disease: VAR_032917
p.LEU223PRO
N/A
N/A
Myopathy, congenital, with fiber-type disproportion (CFTD)


OMIM Disease: 102610.0012
p.LEU221PRO
N/A
N/A
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION






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