ENST00000264414.9:c.1216C>G
MANE Select
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ENSP00000264414.4:p.Gln406Glu
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ENST00000264414.8:c.1216C>G
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ENSP00000264414.4:p.Gln406Glu
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|
ENST00000344951.8:c.1018C>G
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ENSP00000343601.4:p.Gln340Glu
|
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ENST00000409096.5:c.1144C>G
|
ENSP00000387200.1:p.Gln382Glu
|
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ENST00000409777.5:c.1144C>G
|
ENSP00000386525.1:p.Gln382Glu
|
|
ENST00000481135.1:n.512C>G
|
|
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ENST00000617432.4:c.-61C>G
|
ENSP00000477851.1:n.-61C>G
|
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NM_001257197.1:c.1018C>G
|
NP_001244126.1:p.Gln340Glu
|
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NM_001257198.1:c.1234C>G
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NP_001244127.1:p.Gln412Glu
|
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NM_003590.4:c.1216C>G
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NP_003581.1:p.Gln406Glu
|
|
XM_006712800.2:c.1183C>G
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XP_006712863.2:p.Gln395Glu
|
|
XM_011511994.1:c.1069C>G
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XP_011510296.1:p.Gln357Glu
|
|
XM_011511995.1:c.1174C>G
|
XP_011510297.1:p.Gln392Glu
|
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XM_011511996.1:c.1024C>G
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XP_011510298.1:p.Gln342Glu
|
|
XM_011511997.1:c.916C>G
|
XP_011510299.1:p.Gln306Glu
|
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XM_011511994.3:c.1069C>G
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XP_011510296.1:p.Gln357Glu
|
|
XM_011511996.2:c.1024C>G
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XP_011510298.1:p.Gln342Glu
|
|
NM_003590.5:c.1216C>G
MANE Select
|
NP_003581.1:p.Gln406Glu
|
|
NM_001257198.2:c.1234C>G
|
NP_001244127.1:p.Gln412Glu
|
|
NM_001257197.2:c.1018C>G
|
NP_001244126.1:p.Gln340Glu
|
|