ENST00000264414.9:c.1353A>G
MANE Select
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ENSP00000264414.4:p.Glu451=
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ENST00000264414.8:c.1353A>G
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ENSP00000264414.4:p.Glu451=
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|
ENST00000344951.8:c.1155A>G
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ENSP00000343601.4:p.Glu385=
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ENST00000409096.5:c.1281A>G
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ENSP00000387200.1:p.Glu427=
|
|
ENST00000409777.5:c.1281A>G
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ENSP00000386525.1:p.Glu427=
|
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ENST00000481135.1:n.649A>G
|
|
|
ENST00000617432.4:c.77A>G
|
ENSP00000477851.1:p.Lys26Arg
|
|
NM_001257197.1:c.1155A>G
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NP_001244126.1:p.Glu385=
|
|
NM_001257198.1:c.1371A>G
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NP_001244127.1:p.Glu457=
|
|
NM_003590.4:c.1353A>G
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NP_003581.1:p.Glu451=
|
|
XM_006712800.2:c.1320A>G
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XP_006712863.2:p.Glu440=
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|
XM_011511994.1:c.1206A>G
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XP_011510296.1:p.Glu402=
|
|
XM_011511995.1:c.1311A>G
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XP_011510297.1:p.Glu437=
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|
XM_011511996.1:c.1161A>G
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XP_011510298.1:p.Glu387=
|
|
XM_011511997.1:c.1053A>G
|
XP_011510299.1:p.Glu351=
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|
XM_011511994.3:c.1206A>G
|
XP_011510296.1:p.Glu402=
|
|
XM_011511996.2:c.1161A>G
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XP_011510298.1:p.Glu387=
|
|
NM_003590.5:c.1353A>G
MANE Select
|
NP_003581.1:p.Glu451=
|
|
NM_001257198.2:c.1371A>G
|
NP_001244127.1:p.Glu457=
|
|
NM_001257197.2:c.1155A>G
|
NP_001244126.1:p.Glu385=
|
|