ENST00000388913.4:c.816G>T
MANE Select
|
ENSP00000373565.3:p.Glu272Asp
|
|
ENST00000650760.1:c.1419G>T
|
ENSP00000499217.1:p.Glu473Asp
|
|
ENST00000388913.3:c.816G>T
|
ENSP00000373565.3:p.Glu272Asp
|
|
NM_198488.3:c.816G>T
|
NP_940890.3:p.Glu272Asp
|
|
XM_005250887.2:c.873G>T
|
XP_005250944.1:p.Glu291Asp
|
|
XM_005250888.2:c.834G>T
|
XP_005250945.1:p.Glu278Asp
|
|
XM_005250889.2:c.816G>T
|
XP_005250946.1:p.Glu272Asp
|
|
XM_011516980.1:c.1137G>T
|
XP_011515282.1:p.Glu379Asp
|
|
XM_011516981.1:c.984G>T
|
XP_011515283.1:p.Glu328Asp
|
|
XM_005250887.3:c.873G>T
|
XP_005250944.1:p.Glu291Asp
|
|
XM_005250888.3:c.834G>T
|
XP_005250945.1:p.Glu278Asp
|
|
XM_005250889.3:c.816G>T
|
XP_005250946.1:p.Glu272Asp
|
|
XM_011516980.2:c.1419G>T
|
XP_011515282.2:p.Glu473Asp
|
|
XM_011516981.2:c.984G>T
|
XP_011515283.1:p.Glu328Asp
|
|
XM_024447131.1:c.816G>T
|
XP_024302899.1:p.Glu272Asp
|
|
NM_198488.4:c.816G>T
|
NP_940890.3:p.Glu272Asp
|
|
NM_198488.5:c.816G>T
MANE Select
|
NP_940890.4:p.Glu272Asp
|
|