|
ENST00000359206.8:c.863A>T
|
ENSP00000352135.3:p.Glu288Val
|
|
|
ENST00000643670.1:c.879A>T
|
ENSP00000496629.1:n.879A>T
|
|
|
ENST00000644106.1:c.*400A>T
|
ENSP00000493477.1:n.*400A>T
|
|
|
ENST00000649586.2:c.863A>T
MANE Select
|
ENSP00000496956.2:p.Glu288Val
|
|
|
ENST00000265723.8:c.863A>T
|
ENSP00000265723.4:p.Glu288Val
|
|
|
ENST00000358400.7:c.863A>T
|
ENSP00000351172.3:p.Glu288Val
|
|
|
ENST00000359206.7:c.863A>T
|
ENSP00000352135.3:p.Glu288Val
|
|
|
ENST00000453593.5:c.863A>T
|
ENSP00000392983.1:p.Glu288Val
|
|
|
NM_000443.3:c.863A>T
|
NP_000434.1:p.Glu288Val
|
|
|
NM_018849.2:c.863A>T
|
NP_061337.1:p.Glu288Val
|
|
|
NM_018850.2:c.863A>T
|
NP_061338.1:p.Glu288Val
|
|
|
XM_011516308.1:c.863A>T
|
XP_011514610.1:p.Glu288Val
|
|
|
XM_011516309.1:c.863A>T
|
XP_011514611.1:p.Glu288Val
|
|
|
XM_011516310.1:c.863A>T
|
XP_011514612.1:p.Glu288Val
|
|
|
XM_011516311.1:c.863A>T
|
XP_011514613.1:p.Glu288Val
|
|
|
XM_011516312.1:c.863A>T
|
XP_011514614.1:p.Glu288Val
|
|
|
XM_011516313.1:c.863A>T
|
XP_011514615.1:p.Glu288Val
|
|
|
XM_011516314.1:c.884A>T
|
XP_011514616.1:p.Glu295Val
|
|
|
XM_011516315.1:c.203A>T
|
XP_011514617.1:p.Glu68Val
|
|
|
XR_927478.1:n.959A>T
|
|
|
|
XM_011516308.3:c.1133A>T
|
XP_011514610.3:p.Glu378Val
|
|
|
XM_011516309.3:c.1133A>T
|
XP_011514611.3:p.Glu378Val
|
|
|
XM_011516310.3:c.1133A>T
|
XP_011514612.3:p.Glu378Val
|
|
|
XM_011516311.3:c.1133A>T
|
XP_011514613.3:p.Glu378Val
|
|
|
XM_011516312.3:c.1133A>T
|
XP_011514614.3:p.Glu378Val
|
|
|
XM_011516313.3:c.1133A>T
|
XP_011514615.2:p.Glu378Val
|
|
|
XM_011516315.3:c.203A>T
|
XP_011514617.2:p.Glu68Val
|
|
|
XM_017012323.2:c.863A>T
|
XP_016867812.1:p.Glu288Val
|
|
|
XR_001744809.2:n.1634A>T
|
|
|
|
XR_001744810.2:n.1629A>T
|
|
|
|
NM_000443.4:c.863A>T
MANE Select
|
NP_000434.1:p.Glu288Val
|
|
|
NM_018849.3:c.863A>T
|
NP_061337.1:p.Glu288Val
|
|
|
NM_018850.3:c.863A>T
|
NP_061338.1:p.Glu288Val
|
|
