ENST00000216714.8:c.261A>G
MANE Select
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ENSP00000216714.3:p.Glu87=
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ENST00000216714.7:c.261A>G
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ENSP00000216714.3:p.Glu87=
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ENST00000398030.8:c.261A>G
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ENSP00000381111.4:p.Glu87=
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ENST00000438886.1:c.110A>G
|
|
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ENST00000553555.5:n.681A>G
|
|
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ENST00000553681.5:c.261A>G
|
ENSP00000451327.1:p.Glu87=
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ENST00000554325.1:c.*181A>G
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ENSP00000450604.1:n.*181A>G
|
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ENST00000554813.5:n.327A>G
|
|
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ENST00000555306.5:n.708A>G
|
|
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ENST00000555414.5:c.261A>G
|
ENSP00000451979.1:p.Glu87=
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|
ENST00000555839.5:c.261A>G
|
ENSP00000452460.1:p.Glu87=
|
|
ENST00000556054.5:c.261A>G
|
ENSP00000451170.1:p.Glu87=
|
|
ENST00000557054.1:c.28-441A>G
|
ENSP00000452212.2:n.28-441A>G
|
|
ENST00000557150.5:c.210A>G
|
ENSP00000452418.1:p.Glu70=
|
|
ENST00000557159.5:n.877A>G
|
|
|
ENST00000557181.5:c.261A>G
|
ENSP00000452304.1:p.Glu87=
|
|
ENST00000557344.5:c.261A>G
|
ENSP00000452137.1:p.Glu87=
|
|
ENST00000557365.1:n.341A>G
|
|
|
ENST00000557592.5:c.210A>G
|
ENSP00000451060.1:p.Glu70=
|
|
NM_001244249.1:c.261A>G
|
NP_001231178.1:p.Glu87=
|
|
NM_001641.3:c.261A>G
|
NP_001632.2:p.Glu87=
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|
NM_080648.2:c.261A>G
|
NP_542379.1:p.Glu87=
|
|
NM_080649.2:c.261A>G
|
NP_542380.1:p.Glu87=
|
|
XM_005267581.3:c.261A>G
|
XP_005267638.1:p.Glu87=
|
|
XM_005267582.3:c.210A>G
|
XP_005267639.1:p.Glu70=
|
|
NM_001641.4:c.261A>G
MANE Select
|
NP_001632.2:p.Glu87=
|
|
NM_001244249.2:c.261A>G
|
NP_001231178.1:p.Glu87=
|
|
NM_080648.3:c.261A>G
|
NP_542379.1:p.Glu87=
|
|
NM_080649.3:c.261A>G
|
NP_542380.1:p.Glu87=
|
|