ENST00000542218.2:c.638C>A
|
ENSP00000439397.2:p.Thr213Asn
|
|
ENST00000706778.1:c.638C>A
|
ENSP00000516543.1:p.Thr213Asn
|
|
ENST00000706779.1:c.638C>A
|
ENSP00000516544.1:p.Thr213Asn
|
|
ENST00000706780.1:c.638C>A
|
ENSP00000516545.1:p.Thr213Asn
|
|
ENST00000706781.1:c.638C>A
|
ENSP00000516546.1:p.Thr213Asn
|
|
ENST00000706782.1:c.638C>A
|
ENSP00000516547.1:p.Thr213Asn
|
|
ENST00000706783.1:c.469C>A
|
ENSP00000516548.1:p.Pro157Thr
|
|
ENST00000706785.1:c.423C>A
|
ENSP00000516549.1:p.Asp141Glu
|
|
ENST00000706786.1:c.469C>A
|
ENSP00000516550.1:p.Pro157Thr
|
|
ENST00000706787.1:c.638C>A
|
ENSP00000516551.1:p.Thr213Asn
|
|
ENST00000706788.1:n.589C>A
|
|
|
ENST00000376257.8:c.638C>A
MANE Select
|
ENSP00000365433.3:p.Thr213Asn
|
|
ENST00000376255.4:c.638C>A
|
ENSP00000365431.4:p.Thr213Asn
|
|
ENST00000376257.7:c.638C>A
|
ENSP00000365433.3:p.Thr213Asn
|
|
ENST00000496421.1:n.190C>A
|
|
|
ENST00000542218.1:c.398C>A
|
ENSP00000439397.1:p.Thr133Asn
|
|
NM_001077511.1:c.638C>A
|
NP_001070979.1:p.Thr213Asn
|
|
NM_007109.2:c.638C>A
|
NP_009040.2:p.Thr213Asn
|
|
XM_005249334.2:c.638C>A
|
XP_005249391.1:p.Thr213Asn
|
|
XM_011514829.1:c.638C>A
|
XP_011513131.1:p.Thr213Asn
|
|
NM_001318908.1:c.638C>A
|
NP_001305837.1:p.Thr213Asn
|
|
NM_007109.3:c.638C>A
MANE Select
|
NP_009040.2:p.Thr213Asn
|
|
NM_001077511.2:c.638C>A
|
NP_001070979.1:p.Thr213Asn
|
|
NM_001318908.2:c.638C>A
|
NP_001305837.1:p.Thr213Asn
|
|