ENST00000682153.1:c.9807A>C
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ENSP00000507923.1:p.Glu3269Asp
|
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ENST00000682358.1:n.9877A>C
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|
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ENST00000683334.1:c.*5489A>C
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ENSP00000507369.1:n.*5489A>C
|
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ENST00000357162.7:c.9732A>C
MANE Select
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ENSP00000349685.2:p.Glu3244Asp
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ENST00000358544.7:c.9807A>C
MANE Plus Clinical
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ENSP00000351346.2:p.Glu3269Asp
|
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ENST00000357162.6:c.9732A>C
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ENSP00000349685.2:p.Glu3244Asp
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ENST00000358544.6:c.9807A>C
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ENSP00000351346.2:p.Glu3269Asp
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NM_017890.4:c.9807A>C , LRG_351t1:c.9807A>C
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NP_060360.3:p.Glu3269Asp
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NM_152564.4:c.9732A>C , LRG_351t2:c.9732A>C
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NP_689777.3:p.Glu3244Asp
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XM_005250800.2:c.9807A>C
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XP_005250857.1:p.Glu3269Asp
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XM_005250801.3:c.9807A>C
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XP_005250858.1:p.Glu3269Asp
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XM_011516848.1:c.9804A>C
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XP_011515150.1:p.Glu3268Asp
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XM_011516849.1:c.9729A>C
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XP_011515151.1:p.Glu3243Asp
|
|
XM_011516850.1:c.9429A>C
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XP_011515152.1:p.Glu3143Asp
|
|
XM_011516851.1:c.6693A>C
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XP_011515153.1:p.Glu2231Asp
|
|
XM_011516852.1:c.6693A>C
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XP_011515154.1:p.Glu2231Asp
|
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XM_011516854.1:c.5586A>C
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XP_011515156.1:p.Glu1862Asp
|
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XM_005250800.3:c.9807A>C
|
XP_005250857.1:p.Glu3269Asp
|
|
XM_005250801.5:c.9807A>C
|
XP_005250858.1:p.Glu3269Asp
|
|
XM_011516848.2:c.9804A>C
|
XP_011515150.1:p.Glu3268Asp
|
|
XM_011516849.2:c.9729A>C
|
XP_011515151.1:p.Glu3243Asp
|
|
XM_011516850.2:c.9429A>C
|
XP_011515152.1:p.Glu3143Asp
|
|
XM_011516851.2:c.6693A>C
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XP_011515153.1:p.Glu2231Asp
|
|
XM_011516852.2:c.6693A>C
|
XP_011515154.1:p.Glu2231Asp
|
|
XM_011516854.2:c.5586A>C
|
XP_011515156.1:p.Glu1862Asp
|
|
XM_017013109.1:c.9612A>C
|
XP_016868598.1:p.Glu3204Asp
|
|
XM_017013111.1:c.6693A>C
|
XP_016868600.1:p.Glu2231Asp
|
|
XM_017013112.1:c.5364A>C
|
XP_016868601.1:p.Glu1788Asp
|
|
XM_024447074.1:c.8592A>C
|
XP_024302842.1:p.Glu2864Asp
|
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NM_017890.5:c.9807A>C
MANE Plus Clinical
|
NP_060360.3:p.Glu3269Asp
|
|
NM_152564.5:c.9732A>C
MANE Select
|
NP_689777.3:p.Glu3244Asp
|
|