ENST00000233190.11:c.806A>T
MANE Select
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ENSP00000233190.5:p.Glu269Val
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ENST00000233190.10:c.806A>T
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ENSP00000233190.5:p.Glu269Val
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ENST00000423725.5:c.635A>T
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ENSP00000397760.1:p.Glu212Val
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ENST00000432169.5:c.473A>T
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ENSP00000409689.1:p.Glu158Val
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ENST00000440274.5:c.698A>T
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ENSP00000409766.1:p.Glu233Val
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ENST00000449699.5:c.806A>T
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ENSP00000399912.1:p.Glu269Val
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ENST00000455934.6:c.848A>T
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ENSP00000392709.2:p.Glu283Val
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ENST00000457011.5:c.458A>T
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ENSP00000400976.1:p.Glu153Val
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NM_001199981.1:c.698A>T
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NP_001186910.1:p.Glu233Val
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NM_001199982.1:c.473A>T
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NP_001186911.1:p.Glu158Val
|
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NM_001199983.1:c.635A>T
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NP_001186912.1:p.Glu212Val
|
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NM_001199984.1:c.848A>T
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NP_001186913.1:p.Glu283Val
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NM_005006.6:c.806A>T
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NP_004997.4:p.Glu269Val
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XM_017004188.2:c.47A>T
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XP_016859677.1:p.Glu16Val
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NM_001199981.2:c.698A>T
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NP_001186910.1:p.Glu233Val
|
|
NM_001199982.2:c.473A>T
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NP_001186911.1:p.Glu158Val
|
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NM_001199983.2:c.635A>T
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NP_001186912.1:p.Glu212Val
|
|
NM_005006.7:c.806A>T
MANE Select
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NP_004997.4:p.Glu269Val
|
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NM_001199984.2:c.848A>T
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NP_001186913.1:p.Glu283Val
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