ENST00000449291.7:c.1569G>T
MANE Select
|
ENSP00000401508.2:p.Glu523Asp
|
|
ENST00000340490.7:c.1654G>T
|
ENSP00000341136.3:p.Glu552Ter
|
|
ENST00000426292.7:c.1530G>T
|
ENSP00000390949.3:p.Glu510Asp
|
|
ENST00000435154.7:c.*278G>T
|
ENSP00000405670.3:n.*278G>T
|
|
ENST00000449291.6:c.1569G>T
|
ENSP00000401508.2:p.Glu523Asp
|
|
ENST00000460623.5:c.593G>T
|
|
|
ENST00000464332.5:n.1113G>T
|
|
|
ENST00000498076.5:n.348G>T
|
|
|
ENST00000529179.1:n.353G>T
|
|
|
NM_001286829.1:c.1530G>T
|
NP_001273758.1:p.Glu510Asp
|
|
NM_145201.5:c.1569G>T
|
NP_660202.3:p.Glu523Asp
|
|
XM_011517377.1:c.1306G>T
|
XP_011515679.1:p.Glu436Ter
|
|
NM_001363145.1:c.1488G>T
|
NP_001350074.1:p.Glu496Asp
|
|
NM_001363146.1:c.885G>T
|
NP_001350075.1:p.Glu295Asp
|
|
XM_017013975.2:c.1873G>T
|
XP_016869464.1:p.Glu625Ter
|
|
XM_017013976.2:c.1788G>T
|
XP_016869465.1:p.Glu596Asp
|
|
XM_017013977.2:c.1573G>T
|
XP_016869466.1:p.Glu525Ter
|
|
XM_017013978.2:c.1525G>T
|
XP_016869467.1:p.Glu509Ter
|
|
XM_017013979.2:c.970G>T
|
XP_016869468.1:p.Glu324Ter
|
|
XM_024447332.1:c.943G>T
|
XP_024303100.1:p.Glu315Ter
|
|
XM_024447333.1:c.889G>T
|
XP_024303101.1:p.Glu297Ter
|
|
NM_145201.6:c.1569G>T
MANE Select
|
NP_660202.3:p.Glu523Asp
|
|
NM_001286829.2:c.1530G>T
|
NP_001273758.1:p.Glu510Asp
|
|