|
NM_032387.5:c.1459G>A
MANE Select
|
NP_115763.2:p.Glu487Lys
|
|
ENST00000246914.10:c.1459G>A
MANE Select
|
ENSP00000246914.4:p.Glu487Lys
|
|
NM_001321299.1:c.451G>A
|
NP_001308228.1:p.Glu151Lys
|
|
NM_001321299.2:c.451G>A
|
NP_001308228.1:p.Glu151Lys
|
|
NM_032387.4:c.1459G>A
|
NP_115763.2:p.Glu487Lys
|
|
ENST00000246914.9:c.1459G>A
|
ENSP00000246914.4:p.Glu487Lys
|
|
ENST00000587705.5:n.139G>A
|
|
|
ENST00000591448.5:c.1370G>A
|
ENSP00000467088.1:p.Gly457Glu
|
|
ENST00000592072.1:n.139G>A
|
|
|
XM_005257595.3:c.1459G>A
|
XP_005257652.1:p.Glu487Lys
|
|
XM_005257596.2:c.1459G>A
|
XP_005257653.1:p.Glu487Lys
|
|
XM_005257597.3:c.1459G>A
|
XP_005257654.1:p.Glu487Lys
|
|
XM_006722020.2:c.1459G>A
|
XP_006722083.1:p.Glu487Lys
|
|
XM_006722021.1:c.451G>A
|
XP_006722084.1:p.Glu151Lys
|
|
XM_006722022.1:c.451G>A
|
XP_006722085.1:p.Glu151Lys
|
|
XM_011525132.1:c.1459G>A
|
XP_011523434.1:p.Glu487Lys
|
|
XM_011525133.1:c.1459G>A
|
XP_011523435.1:p.Glu487Lys
|
|
XM_011525134.1:c.1459G>A
|
XP_011523436.1:p.Glu487Lys
|
|
XM_011525135.1:c.1459G>A
|
XP_011523437.1:p.Glu487Lys
|
|
XM_017024962.1:c.1459G>A
|
XP_016880451.1:p.Glu487Lys
|
|
XM_017024966.1:c.451G>A
|
XP_016880455.1:p.Glu151Lys
|