ENST00000324856.13:c.5329G>A
MANE Select
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ENSP00000320485.7:p.Glu1777Lys
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ENST00000374152.7:c.4180G>A
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ENSP00000363267.2:p.Glu1394Lys
|
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ENST00000430799.7:c.4177G>A
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ENSP00000390317.3:p.Glu1393Lys
|
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ENST00000466382.2:c.746G>A
|
|
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ENST00000636219.1:c.4183G>A
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ENSP00000489842.1:p.Glu1395Lys
|
|
ENST00000637788.1:n.1129G>A
|
|
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ENST00000324856.11:c.5329G>A
|
ENSP00000320485.7:p.Glu1777Lys
|
|
ENST00000374152.6:c.4180G>A
|
ENSP00000363267.2:p.Glu1394Lys
|
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ENST00000430799.6:c.2018G>A
|
|
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ENST00000457599.6:c.4678G>A
|
ENSP00000387636.2:p.Glu1560Lys
|
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ENST00000466382.1:c.746G>A
|
|
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ENST00000532781.1:c.827G>A
|
|
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NM_006015.4:c.5329G>A , LRG_875t1:c.5329G>A
|
NP_006006.3:p.Glu1777Lys
|
|
NM_139135.2:c.4678G>A
|
NP_624361.1:p.Glu1560Lys
|
|
NM_006015.5:c.5329G>A
|
NP_006006.3:p.Glu1777Lys
|
|
NM_139135.3:c.4678G>A
|
NP_624361.1:p.Glu1560Lys
|
|
NM_006015.6:c.5329G>A
MANE Select
|
NP_006006.3:p.Glu1777Lys
|
|
NM_139135.4:c.4678G>A
|
NP_624361.1:p.Glu1560Lys
|
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