|
ENST00000649042.2:c.288G=
|
ENSP00000497790.2:p.Arg96=
|
|
|
ENST00000649724.2:c.424G=
|
ENSP00000497932.2:p.Glu142=
|
|
|
ENST00000680270.2:c.424G=
|
ENSP00000505532.2:p.Glu142=
|
|
|
ENST00000681056.2:c.46G=
|
ENSP00000506234.2:p.Glu16=
|
|
|
ENST00000368471.8:c.-492G=
|
ENSP00000357456.3:n.-492G=
|
|
|
ENST00000368474.9:c.394G=
MANE Select
|
ENSP00000357459.4:p.Glu132=
|
|
|
ENST00000471068.2:n.391G=
|
|
|
|
ENST00000526905.2:n.258G=
|
|
|
|
ENST00000529168.2:c.394G=
|
ENSP00000431794.2:p.Glu132=
|
|
|
ENST00000647682.2:n.124G=
|
|
|
|
ENST00000648231.2:c.-492G=
|
ENSP00000497555.1:n.-492G=
|
|
|
ENST00000648311.1:c.-492G=
|
ENSP00000498137.1:n.-492G=
|
|
|
ENST00000648714.2:c.394G=
|
ENSP00000497434.2:p.Glu132=
|
|
|
ENST00000648871.1:c.-492G=
|
ENSP00000497793.1:n.-492G=
|
|
|
ENST00000649021.1:n.430G=
|
|
|
|
ENST00000649022.2:c.-492G=
|
ENSP00000496896.2:n.-492G=
|
|
|
ENST00000649042.1:c.-492G=
|
ENSP00000497790.1:n.-492G=
|
|
|
ENST00000649408.2:c.394G=
|
ENSP00000497386.2:p.Glu132=
|
|
|
ENST00000649724.1:c.-492G=
|
ENSP00000497932.1:n.-492G=
|
|
|
ENST00000649749.1:c.-492G=
|
ENSP00000497210.1:n.-492G=
|
|
|
ENST00000679375.1:c.-492G=
|
ENSP00000505887.1:n.-492G=
|
|
|
ENST00000679465.1:n.592G=
|
|
|
|
ENST00000679805.1:n.430G=
|
|
|
|
ENST00000679899.1:c.-492G=
|
ENSP00000505996.1:n.-492G=
|
|
|
ENST00000680270.1:c.-345G=
|
ENSP00000505532.1:n.-345G=
|
|
|
ENST00000680305.1:c.394G=
|
ENSP00000506312.1:p.Glu132=
|
|
|
ENST00000680472.1:n.433G=
|
|
|
|
ENST00000681056.1:c.-492G=
|
ENSP00000506234.1:n.-492G=
|
|
|
ENST00000681235.1:c.258G=
|
ENSP00000506606.1:p.Arg86=
|
|
|
ENST00000681683.1:c.-492G=
|
ENSP00000506666.1:n.-492G=
|
|
|
ENST00000681786.1:n.592G=
|
|
|
|
ENST00000681901.1:c.258G=
|
ENSP00000504883.1:p.Arg86=
|
|
|
ENST00000368471.7:c.-492G=
|
ENSP00000357456.3:n.-492G=
|
|
|
ENST00000368474.8:c.394G=
|
ENSP00000357459.4:p.Glu132=
|
|
|
ENST00000463920.5:n.276G=
|
|
|
|
ENST00000471068.1:n.425G=
|
|
|
|
ENST00000494866.1:n.301G=
|
|
|
|
ENST00000526905.1:n.441G=
|
|
|
|
ENST00000529168.1:c.379G=
|
ENSP00000431794.1:p.Glu127=
|
|
|
NM_001025107.2:c.-492G=
|
NP_001020278.1:n.-492G=
|
|
|
NM_001111.4:c.394G=
|
NP_001102.2:p.Glu132=
|
|
|
NM_001193495.1:c.-492G=
|
NP_001180424.1:n.-492G=
|
|
|
NM_015840.3:c.394G=
|
NP_056655.2:p.Glu132=
|
|
|
NM_015841.3:c.394G=
|
NP_056656.2:p.Glu132=
|
|
|
XM_006711109.1:c.424G=
|
XP_006711172.1:p.Glu142=
|
|
|
XM_006711111.2:c.-492G=
|
XP_006711174.1:n.-492G=
|
|
|
XM_006711112.1:c.-492G=
|
XP_006711175.1:n.-492G=
|
|
|
XM_006711113.1:c.-492G=
|
XP_006711176.1:n.-492G=
|
|
|
XM_011509060.1:c.523G=
|
XP_011507362.1:p.Glu175=
|
|
|
XM_011509061.1:c.523G=
|
XP_011507363.1:p.Glu175=
|
|
|
XM_011509062.1:c.412G=
|
XP_011507364.1:p.Glu138=
|
|
|
NM_001025107.3:c.-492G=
|
NP_001020278.1:n.-492G=
|
|
|
NM_001111.5:c.394G=
MANE Select
|
NP_001102.3:p.Glu132=
|
|
|
NM_001193495.2:c.-492G=
|
NP_001180424.1:n.-492G=
|
|
|
NM_001365045.1:c.421G=
|
NP_001351974.1:p.Glu141=
|
|
|
NM_001365046.1:c.-492G=
|
NP_001351975.1:n.-492G=
|
|
|
NM_001365047.1:c.-492G=
|
NP_001351976.1:n.-492G=
|
|
|
NM_001365048.1:c.-492G=
|
NP_001351977.1:n.-492G=
|
|
|
NM_001365049.1:c.-492G=
|
NP_001351978.1:n.-492G=
|
|
|
NM_015840.4:c.394G=
|
NP_056655.3:p.Glu132=
|
|
|
NM_015841.4:c.394G=
|
NP_056656.3:p.Glu132=
|
|
|
XM_006711113.2:c.-492G=
|
XP_006711176.1:n.-492G=
|
|
|
XM_011509061.2:c.-492G=
|
XP_011507363.2:n.-492G=
|
|
|
XM_024449674.1:c.523G=
|
XP_024305442.1:p.Glu175=
|
|
