ENST00000682153.1:c.5527G>T
|
ENSP00000507923.1:p.Ala1843Ser
|
|
ENST00000682358.1:n.5597G>T
|
|
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ENST00000683334.1:c.*1209G>T
|
ENSP00000507369.1:n.*1209G>T
|
|
ENST00000357162.7:c.5452G>T
MANE Select
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ENSP00000349685.2:p.Ala1818Ser
|
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ENST00000358544.7:c.5527G>T
MANE Plus Clinical
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ENSP00000351346.2:p.Ala1843Ser
|
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ENST00000357162.6:c.5452G>T
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ENSP00000349685.2:p.Ala1818Ser
|
|
ENST00000358544.6:c.5527G>T
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ENSP00000351346.2:p.Ala1843Ser
|
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NM_017890.4:c.5527G>T , LRG_351t1:c.5527G>T
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NP_060360.3:p.Ala1843Ser
|
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NM_152564.4:c.5452G>T , LRG_351t2:c.5452G>T
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NP_689777.3:p.Ala1818Ser
|
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XM_005250800.2:c.5527G>T
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XP_005250857.1:p.Ala1843Ser
|
|
XM_005250801.3:c.5527G>T
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XP_005250858.1:p.Ala1843Ser
|
|
XM_011516848.1:c.5524G>T
|
XP_011515150.1:p.Ala1842Ser
|
|
XM_011516849.1:c.5449G>T
|
XP_011515151.1:p.Ala1817Ser
|
|
XM_011516850.1:c.5149G>T
|
XP_011515152.1:p.Ala1717Ser
|
|
XM_011516851.1:c.2413G>T
|
XP_011515153.1:p.Ala805Ser
|
|
XM_011516852.1:c.2413G>T
|
XP_011515154.1:p.Ala805Ser
|
|
XM_011516853.1:c.5527G>T
|
XP_011515155.1:p.Ala1843Ser
|
|
XM_011516854.1:c.1306G>T
|
XP_011515156.1:p.Ala436Ser
|
|
XM_005250800.3:c.5527G>T
|
XP_005250857.1:p.Ala1843Ser
|
|
XM_005250801.5:c.5527G>T
|
XP_005250858.1:p.Ala1843Ser
|
|
XM_011516848.2:c.5524G>T
|
XP_011515150.1:p.Ala1842Ser
|
|
XM_011516849.2:c.5449G>T
|
XP_011515151.1:p.Ala1817Ser
|
|
XM_011516850.2:c.5149G>T
|
XP_011515152.1:p.Ala1717Ser
|
|
XM_011516851.2:c.2413G>T
|
XP_011515153.1:p.Ala805Ser
|
|
XM_011516852.2:c.2413G>T
|
XP_011515154.1:p.Ala805Ser
|
|
XM_011516853.2:c.5527G>T
|
XP_011515155.1:p.Ala1843Ser
|
|
XM_011516854.2:c.1306G>T
|
XP_011515156.1:p.Ala436Ser
|
|
XM_017013109.1:c.5332G>T
|
XP_016868598.1:p.Ala1778Ser
|
|
XM_017013111.1:c.2413G>T
|
XP_016868600.1:p.Ala805Ser
|
|
XM_017013112.1:c.1084G>T
|
XP_016868601.1:p.Ala362Ser
|
|
XM_024447074.1:c.4312G>T
|
XP_024302842.1:p.Ala1438Ser
|
|
XR_001745482.2:n.5488G>T
|
|
|
NM_017890.5:c.5527G>T
MANE Plus Clinical
|
NP_060360.3:p.Ala1843Ser
|
|
NM_152564.5:c.5452G>T
MANE Select
|
NP_689777.3:p.Ala1818Ser
|
|