|
ENST00000394867.9:n.1619A=
|
|
|
|
ENST00000688002.1:n.3331A=
|
|
|
|
ENST00000688751.1:n.316A=
|
|
|
|
ENST00000689792.1:n.1084A=
|
|
|
|
ENST00000262948.10:c.1180A=
MANE Select
|
ENSP00000262948.4:p.Thr394=
|
|
|
ENST00000262948.9:c.1180A=
|
ENSP00000262948.3:p.Thr394=
|
|
|
ENST00000394867.8:c.889A=
|
ENSP00000378336.1:p.Thr297=
|
|
|
ENST00000597263.5:n.365A=
|
|
|
|
ENST00000599021.1:c.290A=
|
|
|
|
ENST00000600584.5:n.2629A=
|
|
|
|
ENST00000601786.5:n.1481A=
|
|
|
|
NM_030662.3:c.1180A= , LRG_750t1:c.1180A=
|
NP_109587.1:p.Thr394=
|
|
|
XM_006722799.2:c.901A=
|
XP_006722862.1:p.Thr301=
|
|
|
XM_011528133.1:c.610A=
|
XP_011526435.1:p.Thr204=
|
|
|
NM_030662.4:c.1180A=
MANE Select
|
NP_109587.1:p.Thr394=
|
|
