ENST00000706952.1:c.2734G>T
|
ENSP00000516672.1:p.Ala912Ser
|
|
ENST00000638521.1:c.527G>T
|
|
|
ENST00000638869.1:c.36G>T
|
|
|
ENST00000640694.1:c.2575G>T
|
ENSP00000492403.1:p.Ala859Ser
|
|
ENST00000642864.1:c.2575G>T
MANE Select
|
ENSP00000495726.1:p.Ala859Ser
|
|
ENST00000674510.1:c.2575G>T
|
ENSP00000502054.1:p.Ala859Ser
|
|
ENST00000674761.1:n.326G>T
|
|
|
ENST00000675719.1:c.2545G>T
|
ENSP00000501927.1:p.Ala849Ser
|
|
ENST00000375365.2:c.1960G>T
|
ENSP00000364514.2:p.Ala654Ser
|
|
ENST00000396435.7:c.2575G>T
|
ENSP00000379712.3:p.Ala859Ser
|
|
NM_001111125.2:c.2575G>T
|
NP_001104595.1:p.Ala859Ser
|
|
NM_015075.1:c.1960G>T
|
NP_055890.1:p.Ala654Ser
|
|
XM_006724579.2:c.2671G>T
|
XP_006724642.1:p.Ala891Ser
|
|
XM_006724580.2:c.1960G>T
|
XP_006724643.1:p.Ala654Ser
|
|
XM_006724581.2:c.2671G>T
|
XP_006724644.1:p.Ala891Ser
|
|
XM_006724582.2:c.2671G>T
|
XP_006724645.1:p.Ala891Ser
|
|
XM_006724583.2:c.2671G>T
|
XP_006724646.1:p.Ala891Ser
|
|
XM_006724584.2:c.2671G>T
|
XP_006724647.1:p.Ala891Ser
|
|
XM_011530772.1:c.1897G>T
|
XP_011529074.1:p.Ala633Ser
|
|
XM_011530773.1:c.1864G>T
|
XP_011529075.1:p.Ala622Ser
|
|
XM_011530774.1:c.2671G>T
|
XP_011529076.1:p.Ala891Ser
|
|
XM_011530775.1:c.2671G>T
|
XP_011529077.1:p.Ala891Ser
|
|
XM_011530776.1:c.2671G>T
|
XP_011529078.1:p.Ala891Ser
|
|
XM_011530777.1:c.2671G>T
|
XP_011529079.1:p.Ala891Ser
|
|
XR_938365.1:n.2898G>T
|
|
|
XM_006724579.3:c.2671G>T
|
XP_006724642.1:p.Ala891Ser
|
|
XM_006724580.3:c.1960G>T
|
XP_006724643.1:p.Ala654Ser
|
|
XM_006724581.4:c.2671G>T
|
XP_006724644.1:p.Ala891Ser
|
|
XM_006724582.4:c.2671G>T
|
XP_006724645.1:p.Ala891Ser
|
|
XM_006724583.4:c.2671G>T
|
XP_006724646.1:p.Ala891Ser
|
|
XM_006724584.3:c.2671G>T
|
XP_006724647.1:p.Ala891Ser
|
|
XM_011530773.2:c.1864G>T
|
XP_011529075.1:p.Ala622Ser
|
|
XM_011530774.3:c.2671G>T
|
XP_011529076.1:p.Ala891Ser
|
|
XM_011530776.2:c.2671G>T
|
XP_011529078.1:p.Ala891Ser
|
|
XM_011530777.2:c.2671G>T
|
XP_011529079.1:p.Ala891Ser
|
|
XM_017029359.2:c.2545G>T
|
XP_016884848.1:p.Ala849Ser
|
|
XM_017029360.1:c.2077G>T
|
XP_016884849.1:p.Ala693Ser
|
|
XR_938365.2:n.2892G>T
|
|
|
NM_001111125.3:c.2575G>T
MANE Select
|
NP_001104595.1:p.Ala859Ser
|
|
NM_015075.2:c.1960G>T
|
NP_055890.1:p.Ala654Ser
|
|