ENST00000264414.9:c.1272A>G
MANE Select
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ENSP00000264414.4:p.Glu424=
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ENST00000264414.8:c.1272A>G
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ENSP00000264414.4:p.Glu424=
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ENST00000344951.8:c.1074A>G
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ENSP00000343601.4:p.Glu358=
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ENST00000409096.5:c.1200A>G
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ENSP00000387200.1:p.Glu400=
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ENST00000409777.5:c.1200A>G
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ENSP00000386525.1:p.Glu400=
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ENST00000481135.1:n.568A>G
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|
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ENST00000617432.4:c.-5A>G
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ENSP00000477851.1:n.-5A>G
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NM_001257197.1:c.1074A>G
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NP_001244126.1:p.Glu358=
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NM_001257198.1:c.1290A>G
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NP_001244127.1:p.Glu430=
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NM_003590.4:c.1272A>G
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NP_003581.1:p.Glu424=
|
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XM_006712800.2:c.1239A>G
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XP_006712863.2:p.Glu413=
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XM_011511994.1:c.1125A>G
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XP_011510296.1:p.Glu375=
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XM_011511995.1:c.1230A>G
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XP_011510297.1:p.Glu410=
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XM_011511996.1:c.1080A>G
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XP_011510298.1:p.Glu360=
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XM_011511997.1:c.972A>G
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XP_011510299.1:p.Glu324=
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XM_011511994.3:c.1125A>G
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XP_011510296.1:p.Glu375=
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XM_011511996.2:c.1080A>G
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XP_011510298.1:p.Glu360=
|
|
NM_003590.5:c.1272A>G
MANE Select
|
NP_003581.1:p.Glu424=
|
|
NM_001257198.2:c.1290A>G
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NP_001244127.1:p.Glu430=
|
|
NM_001257197.2:c.1074A>G
|
NP_001244126.1:p.Glu358=
|
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