ENST00000361740.9:c.820T>A
|
ENSP00000354468.5:p.Ser274Thr
|
|
ENST00000402438.6:c.619T>A
|
ENSP00000385679.1:p.Ser207Thr
|
|
ENST00000407332.6:c.706T>A
|
ENSP00000384457.2:p.Ser236Thr
|
|
ENST00000407623.8:c.619T>A
|
ENSP00000384834.3:p.Ser207Thr
|
|
ENST00000617178.5:c.225T>A
|
|
|
ENST00000684963.1:n.2428T>A
|
|
|
ENST00000685184.1:n.280T>A
|
|
|
ENST00000686523.1:c.*637T>A
|
ENSP00000508940.1:n.*637T>A
|
|
ENST00000687183.1:n.964T>A
|
|
|
ENST00000687198.1:c.619T>A
|
ENSP00000508492.1:p.Ser207Thr
|
|
ENST00000688117.1:c.787T>A
|
ENSP00000509015.1:p.Ser263Thr
|
|
ENST00000688244.1:c.388T>A
|
ENSP00000510355.1:p.Ser130Thr
|
|
ENST00000689001.1:n.1310T>A
|
|
|
ENST00000689195.1:c.604T>A
|
ENSP00000509895.1:p.Ser202Thr
|
|
ENST00000689239.1:n.855T>A
|
|
|
ENST00000689795.1:n.949T>A
|
|
|
ENST00000690835.1:c.*67T>A
|
ENSP00000509038.1:n.*67T>A
|
|
ENST00000690993.1:n.1443T>A
|
|
|
ENST00000691295.1:c.*171T>A
|
ENSP00000508706.1:n.*171T>A
|
|
ENST00000691918.1:c.978T>A
|
ENSP00000509525.1:n.978T>A
|
|
ENST00000692152.1:c.619T>A
|
ENSP00000509317.1:p.Ser207Thr
|
|
ENST00000692344.1:n.1175T>A
|
|
|
ENST00000693363.1:c.730T>A
|
ENSP00000510411.1:p.Ser244Thr
|
|
ENST00000693367.1:c.688T>A
|
ENSP00000508815.1:p.Ser230Thr
|
|
ENST00000693639.1:c.681T>A
|
ENSP00000510223.1:n.681T>A
|
|
ENST00000693646.1:c.594T>A
|
ENSP00000508449.1:n.594T>A
|
|
ENST00000352397.10:c.688T>A
MANE Select
|
ENSP00000338461.6:p.Ser230Thr
|
|
ENST00000352397.9:c.688T>A
|
ENSP00000338461.6:p.Ser230Thr
|
|
ENST00000361740.8:c.787T>A
|
ENSP00000354468.4:p.Ser263Thr
|
|
ENST00000402438.5:c.619T>A
|
ENSP00000385679.1:p.Ser207Thr
|
|
ENST00000407332.5:c.619T>A
|
ENSP00000384457.1:p.Ser207Thr
|
|
ENST00000407623.7:c.619T>A
|
ENSP00000384834.3:p.Ser207Thr
|
|
ENST00000470741.1:n.2822T>A
|
|
|
NM_000398.6:c.688T>A
|
NP_000389.1:p.Ser230Thr
|
|
NM_001129819.2:c.619T>A
|
NP_001123291.1:p.Ser207Thr
|
|
NM_001171660.1:c.787T>A
|
NP_001165131.1:p.Ser263Thr
|
|
NM_001171661.1:c.619T>A
|
NP_001165132.1:p.Ser207Thr
|
|
NM_007326.4:c.619T>A
|
NP_015565.1:p.Ser207Thr
|
|
NM_000398.7:c.688T>A
MANE Select
|
NP_000389.1:p.Ser230Thr
|
|
NM_001171660.2:c.787T>A
|
NP_001165131.1:p.Ser263Thr
|
|