ENST00000357685.11:c.496G>T
MANE Select
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ENSP00000350314.5:p.Glu166Ter
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ENST00000357685.9:c.496G>T
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ENSP00000350314.5:p.Glu166Ter
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ENST00000361053.8:c.496G>T
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ENSP00000354338.4:p.Glu166Ter
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ENST00000438022.5:c.394G>T
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ENSP00000414843.1:p.Glu132Ter
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ENST00000460924.6:n.588G>T
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ENST00000494860.5:n.348G>T
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ENST00000525987.5:n.839G>T
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ENST00000526088.5:c.394G>T
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ENSP00000436615.1:p.Glu132Ter
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ENST00000527939.1:c.*138G>T
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ENSP00000436956.1:n.*138G>T
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ENST00000530677.1:c.203G>T
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ENST00000531169.5:c.394G>T
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ENSP00000437053.1:p.Glu132Ter
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ENST00000532593.5:c.181G>T
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ENSP00000431802.1:p.Glu61Ter
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ENST00000532612.5:c.426G>T
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ENST00000534122.5:n.1111G>T
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ENST00000534550.5:c.*138G>T
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ENSP00000434488.1:n.*138G>T
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NM_001037290.2:c.394G>T
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NP_001032367.2:p.Glu132Ter
|
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NM_001256397.1:c.394G>T
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NP_001243326.1:p.Glu132Ter
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NM_001256398.1:c.496G>T
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NP_001243327.1:p.Glu166Ter
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NM_001256400.1:c.181G>T
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NP_001243329.1:p.Glu61Ter
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NM_031938.5:c.496G>T
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NP_114144.4:p.Glu166Ter
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NM_001037290.3:c.394G>T
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NP_001032367.3:p.Glu132Ter
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NM_001256397.2:c.394G>T
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NP_001243326.2:p.Glu132Ter
|
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NM_001256398.2:c.496G>T
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NP_001243327.2:p.Glu166Ter
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NM_001256400.2:c.181G>T
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NP_001243329.2:p.Glu61Ter
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NM_031938.7:c.496G>T
MANE Select
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NP_114144.5:p.Glu166Ter
|
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NM_001037290.4:c.394G>T
|
NP_001032367.3:p.Glu132Ter
|
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NM_001256397.3:c.394G>T
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NP_001243326.2:p.Glu132Ter
|
|
NM_001256398.3:c.496G>T
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NP_001243327.2:p.Glu166Ter
|
|
NM_001256400.3:c.181G>T
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NP_001243329.2:p.Glu61Ter
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