ENST00000682153.1:c.7388C>T
|
ENSP00000507923.1:p.Ala2463Val
|
|
ENST00000682358.1:n.7458C>T
|
|
|
ENST00000683334.1:c.*3070C>T
|
ENSP00000507369.1:n.*3070C>T
|
|
ENST00000357162.7:c.7313C>T
MANE Select
|
ENSP00000349685.2:p.Ala2438Val
|
|
ENST00000358544.7:c.7388C>T
MANE Plus Clinical
|
ENSP00000351346.2:p.Ala2463Val
|
|
ENST00000357162.6:c.7313C>T
|
ENSP00000349685.2:p.Ala2438Val
|
|
ENST00000358544.6:c.7388C>T
|
ENSP00000351346.2:p.Ala2463Val
|
|
ENST00000518569.1:n.378-1842C>T
|
|
|
NM_017890.4:c.7388C>T , LRG_351t1:c.7388C>T
|
NP_060360.3:p.Ala2463Val
|
|
NM_152564.4:c.7313C>T , LRG_351t2:c.7313C>T
|
NP_689777.3:p.Ala2438Val
|
|
XM_005250800.2:c.7388C>T
|
XP_005250857.1:p.Ala2463Val
|
|
XM_005250801.3:c.7388C>T
|
XP_005250858.1:p.Ala2463Val
|
|
XM_011516848.1:c.7385C>T
|
XP_011515150.1:p.Ala2462Val
|
|
XM_011516849.1:c.7310C>T
|
XP_011515151.1:p.Ala2437Val
|
|
XM_011516850.1:c.7010C>T
|
XP_011515152.1:p.Ala2337Val
|
|
XM_011516851.1:c.4274C>T
|
XP_011515153.1:p.Ala1425Val
|
|
XM_011516852.1:c.4274C>T
|
XP_011515154.1:p.Ala1425Val
|
|
XM_011516853.1:c.7388C>T
|
XP_011515155.1:p.Ala2463Val
|
|
XM_011516854.1:c.3167C>T
|
XP_011515156.1:p.Ala1056Val
|
|
XR_928446.1:n.1830+5638G>A
|
|
|
XM_005250800.3:c.7388C>T
|
XP_005250857.1:p.Ala2463Val
|
|
XM_005250801.5:c.7388C>T
|
XP_005250858.1:p.Ala2463Val
|
|
XM_011516848.2:c.7385C>T
|
XP_011515150.1:p.Ala2462Val
|
|
XM_011516849.2:c.7310C>T
|
XP_011515151.1:p.Ala2437Val
|
|
XM_011516850.2:c.7010C>T
|
XP_011515152.1:p.Ala2337Val
|
|
XM_011516851.2:c.4274C>T
|
XP_011515153.1:p.Ala1425Val
|
|
XM_011516852.2:c.4274C>T
|
XP_011515154.1:p.Ala1425Val
|
|
XM_011516853.2:c.7388C>T
|
XP_011515155.1:p.Ala2463Val
|
|
XM_011516854.2:c.3167C>T
|
XP_011515156.1:p.Ala1056Val
|
|
XM_017013109.1:c.7193C>T
|
XP_016868598.1:p.Ala2398Val
|
|
XM_017013111.1:c.4274C>T
|
XP_016868600.1:p.Ala1425Val
|
|
XM_017013112.1:c.2945C>T
|
XP_016868601.1:p.Ala982Val
|
|
XM_024447074.1:c.6173C>T
|
XP_024302842.1:p.Ala2058Val
|
|
NM_017890.5:c.7388C>T
MANE Plus Clinical
|
NP_060360.3:p.Ala2463Val
|
|
NM_152564.5:c.7313C>T
MANE Select
|
NP_689777.3:p.Ala2438Val
|
|