ENST00000344887.10:c.186G>C
MANE Select
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ENSP00000341838.5:p.Glu62Asp
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ENST00000665070.1:c.186G>C
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ENSP00000499482.1:p.Glu62Asp
|
|
ENST00000344887.9:c.186G>C
|
ENSP00000341838.5:p.Glu62Asp
|
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ENST00000585806.5:n.185G>C
|
|
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ENST00000586669.5:n.194G>C
|
|
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ENST00000586858.1:c.149G>C
|
ENSP00000465258.1:p.Ser50Thr
|
|
ENST00000587176.5:n.370G>C
|
|
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ENST00000587871.1:c.805G>C
|
|
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ENST00000588882.1:c.111G>C
|
ENSP00000466729.1:p.Glu37Asp
|
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ENST00000590463.1:n.358G>C
|
|
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NM_000363.4:c.186G>C , LRG_432t1:c.186G>C
|
NP_000354.4:p.Glu62Asp
|
|
NM_000363.5:c.186G>C
MANE Select
|
NP_000354.4:p.Glu62Asp
|
|