ENST00000330889.8:c.1044A>G
MANE Select
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ENSP00000329468.3:p.Glu348=
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ENST00000330889.7:c.1044A>G
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ENSP00000329468.3:p.Glu348=
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ENST00000470962.1:n.464A>G
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|
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ENST00000480980.1:n.478A>G
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|
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ENST00000580525.5:c.1062A>G
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ENSP00000464121.1:p.Glu354=
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ENST00000581285.5:c.960A>G
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ENSP00000464155.1:p.Glu320=
|
|
ENST00000584828.5:c.402+11A>G
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|
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ENST00000585130.5:c.*643A>G
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ENSP00000464120.1:n.*643A>G
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NM_018404.2:c.1044A>G
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NP_060874.1:p.Glu348=
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XM_005258008.2:c.1062A>G
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XP_005258065.1:p.Glu354=
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XM_005258011.2:c.999A>G
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XP_005258068.1:p.Glu333=
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|
XM_006721973.2:c.1051+11A>G
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XP_006722036.1:n.1051+11A>G
|
|
XM_011524993.1:c.1059A>G
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XP_011523295.1:p.Glu353=
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|
XM_011524994.1:c.1041A>G
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XP_011523296.1:p.Glu347=
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NM_001346712.1:c.1062A>G
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NP_001333641.1:p.Glu354=
|
|
NM_001346714.1:c.1041A>G
|
NP_001333643.1:p.Glu347=
|
|
NM_001346716.1:c.1033+11A>G
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NP_001333645.1:n.1033+11A>G
|
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NR_144488.1:n.1243A>G
|
|
|
XM_024450831.1:c.1044A>G
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XP_024306599.1:p.Glu348=
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|
XM_024450832.1:c.1059A>G
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XP_024306600.1:p.Glu353=
|
|
XM_024450833.1:c.999A>G
|
XP_024306601.1:p.Glu333=
|
|
XM_024450834.1:c.1051+11A>G
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XP_024306602.1:n.1051+11A>G
|
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XM_024450835.1:c.678A>G
|
XP_024306603.1:p.Glu226=
|
|
NM_018404.3:c.1044A>G
MANE Select
|
NP_060874.1:p.Glu348=
|
|
NM_001346712.2:c.1062A>G
|
NP_001333641.1:p.Glu354=
|
|
NM_001346714.2:c.1041A>G
|
NP_001333643.1:p.Glu347=
|
|
NM_001346716.2:c.1033+11A>G
|
NP_001333645.1:n.1033+11A>G
|
|
NR_144488.2:n.1034A>G
|
|
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