ENST00000706952.1:c.3144G>A
|
ENSP00000516672.1:p.Arg1048=
|
|
ENST00000638521.1:c.937G>A
|
|
|
ENST00000638869.1:c.446G>A
|
|
|
ENST00000639642.1:c.275G>A
|
|
|
ENST00000640005.1:c.48G>A
|
ENSP00000491293.1:p.Arg16=
|
|
ENST00000640694.1:c.2985G>A
|
ENSP00000492403.1:p.Arg995=
|
|
ENST00000642864.1:c.2985G>A
MANE Select
|
ENSP00000495726.1:p.Arg995=
|
|
ENST00000674510.1:c.2985G>A
|
ENSP00000502054.1:p.Arg995=
|
|
ENST00000674761.1:n.1292G>A
|
|
|
ENST00000675719.1:c.2955G>A
|
ENSP00000501927.1:p.Arg985=
|
|
ENST00000375365.2:c.2370G>A
|
ENSP00000364514.2:p.Arg790=
|
|
ENST00000396435.7:c.2985G>A
|
ENSP00000379712.3:p.Arg995=
|
|
NM_001111125.2:c.2985G>A
|
NP_001104595.1:p.Arg995=
|
|
NM_015075.1:c.2370G>A
|
NP_055890.1:p.Arg790=
|
|
XM_006724579.2:c.3081G>A
|
XP_006724642.1:p.Arg1027=
|
|
XM_006724580.2:c.2370G>A
|
XP_006724643.1:p.Arg790=
|
|
XM_006724581.2:c.3081G>A
|
XP_006724644.1:p.Arg1027=
|
|
XM_006724582.2:c.3081G>A
|
XP_006724645.1:p.Arg1027=
|
|
XM_006724583.2:c.3081G>A
|
XP_006724646.1:p.Arg1027=
|
|
XM_006724584.2:c.3081G>A
|
XP_006724647.1:p.Arg1027=
|
|
XM_011530772.1:c.2307G>A
|
XP_011529074.1:p.Arg769=
|
|
XM_011530773.1:c.2274G>A
|
XP_011529075.1:p.Arg758=
|
|
XM_011530774.1:c.3081G>A
|
XP_011529076.1:p.Arg1027=
|
|
XM_011530775.1:c.3081G>A
|
XP_011529077.1:p.Arg1027=
|
|
XM_011530776.1:c.3081G>A
|
XP_011529078.1:p.Arg1027=
|
|
XM_011530777.1:c.3081G>A
|
XP_011529079.1:p.Arg1027=
|
|
XR_938365.1:n.3308G>A
|
|
|
XM_006724579.3:c.3081G>A
|
XP_006724642.1:p.Arg1027=
|
|
XM_006724580.3:c.2370G>A
|
XP_006724643.1:p.Arg790=
|
|
XM_006724581.4:c.3081G>A
|
XP_006724644.1:p.Arg1027=
|
|
XM_006724582.4:c.3081G>A
|
XP_006724645.1:p.Arg1027=
|
|
XM_006724583.4:c.3081G>A
|
XP_006724646.1:p.Arg1027=
|
|
XM_006724584.3:c.3081G>A
|
XP_006724647.1:p.Arg1027=
|
|
XM_011530773.2:c.2274G>A
|
XP_011529075.1:p.Arg758=
|
|
XM_011530774.3:c.3081G>A
|
XP_011529076.1:p.Arg1027=
|
|
XM_011530776.2:c.3081G>A
|
XP_011529078.1:p.Arg1027=
|
|
XM_011530777.2:c.3081G>A
|
XP_011529079.1:p.Arg1027=
|
|
XM_017029359.2:c.2955G>A
|
XP_016884848.1:p.Arg985=
|
|
XM_017029360.1:c.2487G>A
|
XP_016884849.1:p.Arg829=
|
|
XR_938365.2:n.3302G>A
|
|
|
NM_001111125.3:c.2985G>A
MANE Select
|
NP_001104595.1:p.Arg995=
|
|
NM_015075.2:c.2370G>A
|
NP_055890.1:p.Arg790=
|
|