ENST00000260947.9:c.972T>C
MANE Select
|
ENSP00000260947.4:p.His324=
|
|
ENST00000421162.2:c.215+16159T>C
|
ENSP00000392245.2:n.215+16159T>C
|
|
ENST00000613192.2:c.158+28510T>C
|
ENSP00000483275.2:n.158+28510T>C
|
|
ENST00000613374.5:c.159-28347T>C
|
ENSP00000484464.1:n.159-28347T>C
|
|
ENST00000613706.5:c.906+66T>C
|
ENSP00000484976.2:n.906+66T>C
|
|
ENST00000617164.5:c.915T>C
|
ENSP00000480470.1:p.His305=
|
|
ENST00000619009.5:c.364+11395T>C
|
ENSP00000482293.1:n.364+11395T>C
|
|
ENST00000650978.1:c.814T>C
|
|
|
ENST00000260947.8:c.972T>C
|
ENSP00000260947.4:p.His324=
|
|
ENST00000421162.1:c.215+16159T>C
|
ENSP00000392245.1:n.215+16159T>C
|
|
ENST00000455743.5:c.*592T>C
|
ENSP00000412186.1:n.*592T>C
|
|
ENST00000471787.1:n.867T>C
|
|
|
ENST00000613192.1:c.73+28510T>C
|
ENSP00000483275.1:n.73+28510T>C
|
|
ENST00000613374.4:c.159-28347T>C
|
ENSP00000484464.1:n.159-28347T>C
|
|
ENST00000613706.4:c.215+16159T>C
|
ENSP00000484976.1:n.215+16159T>C
|
|
ENST00000617164.4:c.915T>C
|
ENSP00000480470.1:p.His305=
|
|
ENST00000619009.4:c.364+11395T>C
|
ENSP00000482293.1:n.364+11395T>C
|
|
ENST00000620057.4:c.364+11395T>C
|
ENSP00000481988.1:n.364+11395T>C
|
|
NM_000465.3:c.972T>C
|
NP_000456.2:p.His324=
|
|
NM_001282543.1:c.915T>C
|
NP_001269472.1:p.His305=
|
|
NM_001282545.1:c.215+16159T>C
|
NP_001269474.1:n.215+16159T>C
|
|
NM_001282548.1:c.159-28347T>C
|
NP_001269477.1:n.159-28347T>C
|
|
NM_001282549.1:c.364+11395T>C
|
NP_001269478.1:n.364+11395T>C
|
|
NR_104212.1:n.965T>C
|
|
|
NR_104215.1:n.908T>C
|
|
|
NR_104216.1:n.506+11395T>C
|
|
|
XM_011511567.1:c.918T>C
|
XP_011509869.1:p.His306=
|
|
XM_011511568.1:c.972T>C
|
XP_011509870.1:p.His324=
|
|
XM_017004613.1:c.1071T>C
|
XP_016860102.1:p.His357=
|
|
XM_017004614.1:c.1071T>C
|
XP_016860103.1:p.His357=
|
|
XR_002959322.1:n.1162T>C
|
|
|
NM_000465.4:c.972T>C
MANE Select
|
NP_000456.2:p.His324=
|
|
NM_001282543.2:c.915T>C
|
NP_001269472.1:p.His305=
|
|
NM_001282545.2:c.215+16159T>C
|
NP_001269474.1:n.215+16159T>C
|
|
NM_001282548.2:c.159-28347T>C
|
NP_001269477.1:n.159-28347T>C
|
|
NM_001282549.2:c.364+11395T>C
|
NP_001269478.1:n.364+11395T>C
|
|
NR_104212.2:n.937T>C
|
|
|
NR_104215.2:n.880T>C
|
|
|
NR_104216.2:n.478+11395T>C
|
|
|