ENST00000449291.7:c.1455G>C
MANE Select
|
ENSP00000401508.2:p.Glu485Asp
|
|
ENST00000340490.7:c.1455G>C
|
ENSP00000341136.3:p.Glu485Asp
|
|
ENST00000426292.7:c.1416G>C
|
ENSP00000390949.3:p.Glu472Asp
|
|
ENST00000435154.7:c.*79G>C
|
ENSP00000405670.3:n.*79G>C
|
|
ENST00000449291.6:c.1455G>C
|
ENSP00000401508.2:p.Glu485Asp
|
|
ENST00000460623.5:c.394G>C
|
|
|
ENST00000464332.5:n.999G>C
|
|
|
ENST00000498076.5:n.234G>C
|
|
|
ENST00000529179.1:n.239G>C
|
|
|
NM_001286829.1:c.1416G>C
|
NP_001273758.1:p.Glu472Asp
|
|
NM_145201.5:c.1455G>C
|
NP_660202.3:p.Glu485Asp
|
|
XM_011517377.1:c.1292-185G>C
|
XP_011515679.1:n.1292-185G>C
|
|
NM_001363145.1:c.1374G>C
|
NP_001350074.1:p.Glu458Asp
|
|
NM_001363146.1:c.771G>C
|
NP_001350075.1:p.Glu257Asp
|
|
XM_017013975.2:c.1674G>C
|
XP_016869464.1:p.Glu558Asp
|
|
XM_017013976.2:c.1674G>C
|
XP_016869465.1:p.Glu558Asp
|
|
XM_017013977.2:c.1374G>C
|
XP_016869466.1:p.Glu458Asp
|
|
XM_017013978.2:c.1511-185G>C
|
XP_016869467.1:n.1511-185G>C
|
|
XM_017013979.2:c.771G>C
|
XP_016869468.1:p.Glu257Asp
|
|
XM_024447332.1:c.929-185G>C
|
XP_024303100.1:n.929-185G>C
|
|
XM_024447333.1:c.690G>C
|
XP_024303101.1:p.Glu230Asp
|
|
NM_145201.6:c.1455G>C
MANE Select
|
NP_660202.3:p.Glu485Asp
|
|
NM_001286829.2:c.1416G>C
|
NP_001273758.1:p.Glu472Asp
|
|