ENST00000276072.9:c.2956G>A
|
ENSP00000276072.5:p.Glu986Lys
|
|
ENST00000483985.3:c.585G>A
|
|
|
ENST00000683202.1:c.3670G>A
|
ENSP00000507781.1:p.Glu1224Lys
|
|
ENST00000683668.1:c.2956G>A
|
ENSP00000507280.1:p.Glu986Lys
|
|
ENST00000683782.1:c.3670G>A
|
ENSP00000506996.1:p.Glu1224Lys
|
|
ENST00000276072.8:c.264G>A
|
|
|
ENST00000373790.9:c.3607G>A
|
ENSP00000362895.5:p.Glu1203Lys
|
|
ENST00000423759.6:c.3670G>A
MANE Select
|
ENSP00000406549.2:p.Glu1224Lys
|
|
ENST00000276072.7:c.3730G>A
|
ENSP00000276072.3:p.Glu1244Lys
|
|
ENST00000373790.8:c.3667G>A
|
ENSP00000362895.4:p.Glu1223Lys
|
|
ENST00000423759.5:c.3730G>A
|
ENSP00000406549.1:p.Glu1244Lys
|
|
ENST00000483985.2:c.399G>A
|
|
|
NM_001286074.1:c.3730G>A
|
NP_001273003.1:p.Glu1244Lys
|
|
NM_004606.4:c.3730G>A
|
NP_004597.2:p.Glu1244Lys
|
|
NM_138923.3:c.3667G>A
|
NP_620278.1:p.Glu1223Lys
|
|
NR_104387.1:n.3806G>A
|
|
|
NR_104388.1:n.3806G>A
|
|
|
NR_104389.1:n.3806G>A
|
|
|
NR_104390.1:n.3806G>A
|
|
|
NR_104391.1:n.3806G>A
|
|
|
NR_104392.1:n.3806G>A
|
|
|
NR_104393.1:n.3806G>A
|
|
|
NR_104394.1:n.3806G>A
|
|
|
NR_104395.1:n.3806G>A
|
|
|
XM_005262295.1:c.3730G>A
|
XP_005262352.1:p.Glu1244Lys
|
|
XM_005262296.1:c.3727G>A
|
XP_005262353.1:p.Glu1243Lys
|
|
XM_005262297.3:c.3667G>A
|
XP_005262354.1:p.Glu1223Lys
|
|
XM_006724682.2:c.3349G>A
|
XP_006724745.1:p.Glu1117Lys
|
|
XM_011531016.1:c.3730G>A
|
XP_011529318.1:p.Glu1244Lys
|
|
XR_938407.1:n.3740G>A
|
|
|
XM_005262297.4:c.3667G>A
|
XP_005262354.1:p.Glu1223Lys
|
|
XM_024452429.1:c.3349G>A
|
XP_024308197.1:p.Glu1117Lys
|
|
XM_024452430.1:c.3730G>A
|
XP_024308198.1:p.Glu1244Lys
|
|
NM_001286074.2:c.3670G>A
|
NP_001273003.2:p.Glu1224Lys
|
|
NM_004606.5:c.3670G>A
MANE Select
|
NP_004597.3:p.Glu1224Lys
|
|
NM_138923.4:c.3607G>A
|
NP_620278.2:p.Glu1203Lys
|
|
NR_104387.2:n.3688G>A
|
|
|
NR_104388.2:n.3688G>A
|
|
|
NR_104389.2:n.3688G>A
|
|
|
NR_104390.2:n.3688G>A
|
|
|
NR_104391.2:n.3688G>A
|
|
|
NR_104392.2:n.3688G>A
|
|
|
NR_104393.2:n.3688G>A
|
|
|
NR_104394.2:n.3688G>A
|
|
|
NR_104395.2:n.3688G>A
|
|
|