ENST00000324856.13:c.5324A>G
MANE Select
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ENSP00000320485.7:p.Glu1775Gly
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ENST00000374152.7:c.4175A>G
|
ENSP00000363267.2:p.Glu1392Gly
|
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ENST00000430799.7:c.4172A>G
|
ENSP00000390317.3:p.Glu1391Gly
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ENST00000466382.2:c.741A>G
|
|
|
ENST00000636219.1:c.4178A>G
|
ENSP00000489842.1:p.Glu1393Gly
|
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ENST00000637788.1:n.1124A>G
|
|
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ENST00000324856.11:c.5324A>G
|
ENSP00000320485.7:p.Glu1775Gly
|
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ENST00000374152.6:c.4175A>G
|
ENSP00000363267.2:p.Glu1392Gly
|
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ENST00000430799.6:c.2013A>G
|
|
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ENST00000457599.6:c.4673A>G
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ENSP00000387636.2:p.Glu1558Gly
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ENST00000466382.1:c.741A>G
|
|
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ENST00000532781.1:c.822A>G
|
|
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NM_006015.4:c.5324A>G , LRG_875t1:c.5324A>G
|
NP_006006.3:p.Glu1775Gly
|
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NM_139135.2:c.4673A>G
|
NP_624361.1:p.Glu1558Gly
|
|
NM_006015.5:c.5324A>G
|
NP_006006.3:p.Glu1775Gly
|
|
NM_139135.3:c.4673A>G
|
NP_624361.1:p.Glu1558Gly
|
|
NM_006015.6:c.5324A>G
MANE Select
|
NP_006006.3:p.Glu1775Gly
|
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NM_139135.4:c.4673A>G
|
NP_624361.1:p.Glu1558Gly
|
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