ENST00000621392.5:c.747C>A
MANE Select
|
ENSP00000477573.2:p.Thr249=
|
|
ENST00000315184.9:c.747C>A
|
ENSP00000326652.4:p.Thr249=
|
|
ENST00000466842.1:c.315C>A
|
ENSP00000417930.1:p.Thr105=
|
|
ENST00000469348.5:n.606C>A
|
|
|
ENST00000471558.5:c.747C>A
|
ENSP00000418672.1:p.Thr249=
|
|
ENST00000484425.6:c.318C>A
|
ENSP00000418591.2:p.Thr106=
|
|
ENST00000485070.5:c.450C>A
|
ENSP00000418192.1:p.Thr150=
|
|
ENST00000493738.5:n.703C>A
|
|
|
ENST00000621392.4:c.450C>A
|
ENSP00000477573.1:p.Thr150=
|
|
NM_001282788.1:c.747C>A
|
NP_001269717.1:p.Thr249=
|
|
NM_001282789.1:c.450C>A
|
NP_001269718.1:p.Thr150=
|
|
NM_032599.3:c.747C>A
|
NP_115988.1:p.Thr249=
|
|
NR_104242.1:n.847C>A
|
|
|
NR_104243.1:n.736C>A
|
|
|
XM_017012743.2:c.747C>A
|
XP_016868232.1:p.Thr249=
|
|
XR_002956499.1:n.798C>A
|
|
|
NM_001282788.2:c.747C>A
|
NP_001269717.1:p.Thr249=
|
|
NM_001282789.2:c.450C>A
|
NP_001269718.1:p.Thr150=
|
|
NM_032599.4:c.747C>A
|
NP_115988.1:p.Thr249=
|
|
NR_104242.2:n.798C>A
|
|
|
NR_104243.2:n.736C>A
|
|
|
NM_001282788.3:c.747C>A
MANE Select
|
NP_001269717.1:p.Thr249=
|
|