ENST00000394867.9:n.1456C>A
|
|
|
ENST00000688002.1:n.3168C>A
|
|
|
ENST00000688751.1:n.153C>A
|
|
|
ENST00000689792.1:n.921C>A
|
|
|
ENST00000262948.10:c.1017C>A
MANE Select
|
ENSP00000262948.4:p.Thr339=
|
|
ENST00000262948.9:c.1017C>A
|
ENSP00000262948.3:p.Thr339=
|
|
ENST00000394867.8:c.726C>A
|
ENSP00000378336.1:p.Thr242=
|
|
ENST00000595715.1:n.832C>A
|
|
|
ENST00000597263.5:n.202C>A
|
|
|
ENST00000599021.1:c.127C>A
|
|
|
ENST00000600584.5:n.1577C>A
|
|
|
ENST00000601786.5:n.1318C>A
|
|
|
NM_030662.3:c.1017C>A , LRG_750t1:c.1017C>A
|
NP_109587.1:p.Thr339=
|
|
XM_006722799.2:c.738C>A
|
XP_006722862.1:p.Thr246=
|
|
XM_011528133.1:c.447C>A
|
XP_011526435.1:p.Thr149=
|
|
XM_017026989.1:c.1017C>A
|
XP_016882478.1:p.Thr339=
|
|
XM_017026990.1:c.738C>A
|
XP_016882479.1:p.Thr246=
|
|
NM_030662.4:c.1017C>A
MANE Select
|
NP_109587.1:p.Thr339=
|
|