|
ENST00000333646.11:c.4094G>C
|
ENSP00000333125.8:p.Ser1365Thr
|
|
|
ENST00000374102.6:c.4214G>C
|
ENSP00000363215.2:p.Ser1405Thr
|
|
|
ENST00000685182.1:n.847G>C
|
|
|
|
ENST00000685655.1:c.167G>C
|
ENSP00000509298.1:p.Ser56Thr
|
|
|
ENST00000686169.1:n.591G>C
|
|
|
|
ENST00000686548.1:c.*4110G>C
|
ENSP00000509582.1:n.*4110G>C
|
|
|
ENST00000687161.1:n.929G>C
|
|
|
|
ENST00000687382.1:c.4214G>C
|
ENSP00000510724.1:p.Ser1405Thr
|
|
|
ENST00000687701.1:n.843G>C
|
|
|
|
ENST00000688079.1:n.2209G>C
|
|
|
|
ENST00000688663.1:c.*1135G>C
|
ENSP00000509348.1:n.*1135G>C
|
|
|
ENST00000688881.1:n.868G>C
|
|
|
|
ENST00000688993.1:n.415G>C
|
|
|
|
ENST00000689768.1:n.2824G>C
|
|
|
|
ENST00000690145.1:c.4214G>C
|
ENSP00000508818.1:p.Ser1405Thr
|
|
|
ENST00000690242.1:c.4214G>C
|
ENSP00000510090.1:p.Ser1405Thr
|
|
|
ENST00000690250.1:n.1883G>C
|
|
|
|
ENST00000690690.1:c.667G>C
|
|
|
|
ENST00000690828.1:n.4470G>C
|
|
|
|
ENST00000691113.1:c.2693G>C
|
ENSP00000509755.1:n.2693G>C
|
|
|
ENST00000691426.1:n.3343G>C
|
|
|
|
ENST00000691468.1:c.4163G>C
|
ENSP00000509011.1:p.Ser1388Thr
|
|
|
ENST00000691909.1:n.934G>C
|
|
|
|
ENST00000692304.1:c.4214G>C
|
ENSP00000508427.1:p.Ser1405Thr
|
|
|
ENST00000692893.1:n.1523G>C
|
|
|
|
ENST00000692964.1:n.878G>C
|
|
|
|
ENST00000693050.1:n.721G>C
|
|
|
|
ENST00000693324.1:c.4178G>C
|
ENSP00000508643.1:p.Ser1393Thr
|
|
|
ENST00000693391.1:c.2159G>C
|
ENSP00000509563.1:p.Ser720Thr
|
|
|
ENST00000374080.8:c.4214G>C
MANE Select
|
ENSP00000363193.3:p.Ser1405Thr
|
|
|
ENST00000333646.10:c.3755G>C
|
ENSP00000333125.7:p.Ser1252Thr
|
|
|
ENST00000374080.7:c.4214G>C
|
ENSP00000363193.3:p.Ser1405Thr
|
|
|
ENST00000374102.5:c.4214G>C
|
ENSP00000363215.1:p.Ser1405Thr
|
|
|
NM_005120.2:c.4214G>C
|
NP_005111.2:p.Ser1405Thr
|
|
|
XM_005262317.1:c.4214G>C
|
XP_005262374.1:p.Ser1405Thr
|
|
|
XM_005262319.1:c.4214G>C
|
XP_005262376.1:p.Ser1405Thr
|
|
|
NM_005120.3:c.4214G>C
MANE Select
|
NP_005111.2:p.Ser1405Thr
|
|
