ENST00000394867.9:n.1172T>A
|
|
|
ENST00000687128.1:n.1172T>A
|
|
|
ENST00000688002.1:n.1027T>A
|
|
|
ENST00000689792.1:n.646-9T>A
|
|
|
ENST00000262948.10:c.733T>A
MANE Select
|
ENSP00000262948.4:p.Ser245Thr
|
|
ENST00000262948.9:c.733T>A
|
ENSP00000262948.3:p.Ser245Thr
|
|
ENST00000394867.8:c.442T>A
|
ENSP00000378336.1:p.Ser148Thr
|
|
ENST00000593364.5:n.680T>A
|
|
|
ENST00000595715.1:n.548T>A
|
|
|
ENST00000597263.5:n.169+1632T>A
|
|
|
ENST00000599021.1:c.29+1632T>A
|
|
|
ENST00000600584.5:n.1293T>A
|
|
|
ENST00000601786.5:n.1034T>A
|
|
|
NM_030662.3:c.733T>A , LRG_750t1:c.733T>A
|
NP_109587.1:p.Ser245Thr
|
|
XM_006722799.2:c.705+1632T>A
|
XP_006722862.1:n.705+1632T>A
|
|
XM_011528133.1:c.163T>A
|
XP_011526435.1:p.Ser55Thr
|
|
XM_017026989.1:c.733T>A
|
XP_016882478.1:p.Ser245Thr
|
|
XM_017026990.1:c.705+1632T>A
|
XP_016882479.1:n.705+1632T>A
|
|
NM_030662.4:c.733T>A
MANE Select
|
NP_109587.1:p.Ser245Thr
|
|