ENST00000682153.1:c.7461C>T
|
ENSP00000507923.1:p.His2487=
|
|
ENST00000682358.1:n.7531C>T
|
|
|
ENST00000683334.1:c.*3143C>T
|
ENSP00000507369.1:n.*3143C>T
|
|
ENST00000357162.7:c.7386C>T
MANE Select
|
ENSP00000349685.2:p.His2462=
|
|
ENST00000358544.7:c.7461C>T
MANE Plus Clinical
|
ENSP00000351346.2:p.His2487=
|
|
ENST00000357162.6:c.7386C>T
|
ENSP00000349685.2:p.His2462=
|
|
ENST00000358544.6:c.7461C>T
|
ENSP00000351346.2:p.His2487=
|
|
ENST00000518569.1:n.378-1769C>T
|
|
|
NM_017890.4:c.7461C>T , LRG_351t1:c.7461C>T
|
NP_060360.3:p.His2487=
|
|
NM_152564.4:c.7386C>T , LRG_351t2:c.7386C>T
|
NP_689777.3:p.His2462=
|
|
XM_005250800.2:c.7461C>T
|
XP_005250857.1:p.His2487=
|
|
XM_005250801.3:c.7461C>T
|
XP_005250858.1:p.His2487=
|
|
XM_011516848.1:c.7458C>T
|
XP_011515150.1:p.His2486=
|
|
XM_011516849.1:c.7383C>T
|
XP_011515151.1:p.His2461=
|
|
XM_011516850.1:c.7083C>T
|
XP_011515152.1:p.His2361=
|
|
XM_011516851.1:c.4347C>T
|
XP_011515153.1:p.His1449=
|
|
XM_011516852.1:c.4347C>T
|
XP_011515154.1:p.His1449=
|
|
XM_011516853.1:c.7461C>T
|
XP_011515155.1:p.His2487=
|
|
XM_011516854.1:c.3240C>T
|
XP_011515156.1:p.His1080=
|
|
XR_928446.1:n.1830+5565G>A
|
|
|
XM_005250800.3:c.7461C>T
|
XP_005250857.1:p.His2487=
|
|
XM_005250801.5:c.7461C>T
|
XP_005250858.1:p.His2487=
|
|
XM_011516848.2:c.7458C>T
|
XP_011515150.1:p.His2486=
|
|
XM_011516849.2:c.7383C>T
|
XP_011515151.1:p.His2461=
|
|
XM_011516850.2:c.7083C>T
|
XP_011515152.1:p.His2361=
|
|
XM_011516851.2:c.4347C>T
|
XP_011515153.1:p.His1449=
|
|
XM_011516852.2:c.4347C>T
|
XP_011515154.1:p.His1449=
|
|
XM_011516853.2:c.7461C>T
|
XP_011515155.1:p.His2487=
|
|
XM_011516854.2:c.3240C>T
|
XP_011515156.1:p.His1080=
|
|
XM_017013109.1:c.7266C>T
|
XP_016868598.1:p.His2422=
|
|
XM_017013111.1:c.4347C>T
|
XP_016868600.1:p.His1449=
|
|
XM_017013112.1:c.3018C>T
|
XP_016868601.1:p.His1006=
|
|
XM_024447074.1:c.6246C>T
|
XP_024302842.1:p.His2082=
|
|
NM_017890.5:c.7461C>T
MANE Plus Clinical
|
NP_060360.3:p.His2487=
|
|
NM_152564.5:c.7386C>T
MANE Select
|
NP_689777.3:p.His2462=
|
|