ENST00000369409.9:c.418G>T
|
ENSP00000358417.5:p.Gly140Ter
|
|
ENST00000462324.2:n.501G>T
|
|
|
ENST00000641023.2:c.418G>T
MANE Select
|
ENSP00000493175.1:p.Gly140Ter
|
|
ENST00000641074.1:c.418G>T
|
ENSP00000493446.1:p.Gly140Ter
|
|
ENST00000641115.1:c.418G>T
|
ENSP00000493264.1:p.Gly140Ter
|
|
ENST00000641213.1:c.*71G>T
|
ENSP00000493079.1:n.*71G>T
|
|
ENST00000641247.1:c.*137G>T
|
ENSP00000492955.1:n.*137G>T
|
|
ENST00000641272.1:c.352G>T
|
ENSP00000493432.1:p.Gly118Ter
|
|
ENST00000641314.1:n.403G>T
|
|
|
ENST00000641371.1:c.332G>T
|
ENSP00000493305.1:p.Gly111Val
|
|
ENST00000641375.1:c.*254G>T
|
ENSP00000493089.1:n.*254G>T
|
|
ENST00000641491.1:c.*71G>T
|
ENSP00000493187.1:n.*71G>T
|
|
ENST00000641570.1:c.*137G>T
|
ENSP00000493213.1:n.*137G>T
|
|
ENST00000641573.1:n.506G>T
|
|
|
ENST00000641587.1:c.*129G>T
|
ENSP00000493453.1:n.*129G>T
|
|
ENST00000641597.1:c.418G>T
|
ENSP00000493382.1:p.Gly140Ter
|
|
ENST00000641711.1:n.642G>T
|
|
|
ENST00000641756.1:c.*162G>T
|
ENSP00000493147.1:n.*162G>T
|
|
ENST00000641811.1:c.174G>T
|
|
|
ENST00000641847.1:n.277G>T
|
|
|
ENST00000641891.1:c.*244G>T
|
ENSP00000493288.1:n.*244G>T
|
|
ENST00000641927.1:n.358G>T
|
|
|
ENST00000641947.1:c.418G>T
|
ENSP00000492994.1:p.Gly140Ter
|
|
ENST00000642021.1:n.540G>T
|
|
|
ENST00000642041.1:c.*457G>T
|
ENSP00000493415.1:n.*457G>T
|
|
ENST00000369407.3:c.316G>T
|
ENSP00000358415.3:p.Gly106Ter
|
|
ENST00000369409.8:c.418G>T
|
ENSP00000358417.4:p.Gly140Ter
|
|
ENST00000462324.1:n.686G>T
|
|
|
ENST00000493622.5:n.607G>T
|
|
|
NM_006623.3:c.418G>T
|
NP_006614.2:p.Gly140Ter
|
|
XM_011541226.1:c.640G>T
|
XP_011539528.1:p.Gly214Ter
|
|
XM_011541227.1:c.562G>T
|
XP_011539529.1:p.Gly188Ter
|
|
XM_011541228.1:c.529G>T
|
XP_011539530.1:p.Gly177Ter
|
|
XM_011541229.1:c.355G>T
|
XP_011539531.1:p.Gly119Ter
|
|
XM_011541230.1:c.133G>T
|
XP_011539532.1:p.Gly45Ter
|
|
XM_011541231.1:c.124G>T
|
XP_011539533.1:p.Gly42Ter
|
|
XM_011541226.2:c.640G>T
|
XP_011539528.1:p.Gly214Ter
|
|
XM_011541227.2:c.562G>T
|
XP_011539529.1:p.Gly188Ter
|
|
XM_011541228.2:c.529G>T
|
XP_011539530.1:p.Gly177Ter
|
|
XM_011541231.2:c.124G>T
|
XP_011539533.1:p.Gly42Ter
|
|
XM_024446338.1:c.529G>T
|
XP_024302106.1:p.Gly177Ter
|
|
NM_006623.4:c.418G>T
MANE Select
|
NP_006614.2:p.Gly140Ter
|
|