ENST00000394867.9:n.1632C=
|
|
|
ENST00000688002.1:n.3344C=
|
|
|
ENST00000688751.1:n.329C=
|
|
|
ENST00000689792.1:n.1097C=
|
|
|
ENST00000262948.10:c.1193C=
MANE Select
|
ENSP00000262948.4:p.Thr398=
|
|
ENST00000262948.9:c.1193C=
|
ENSP00000262948.3:p.Thr398=
|
|
ENST00000394867.8:c.902C=
|
ENSP00000378336.1:p.Thr301=
|
|
ENST00000597263.5:n.378C=
|
|
|
ENST00000599021.1:c.303C=
|
|
|
ENST00000600584.5:n.2642C=
|
|
|
ENST00000601786.5:n.1494C=
|
|
|
NM_030662.3:c.1193C= , LRG_750t1:c.1193C=
|
NP_109587.1:p.Thr398=
|
|
XM_006722799.2:c.914C=
|
XP_006722862.1:p.Thr305=
|
|
XM_011528133.1:c.623C=
|
XP_011526435.1:p.Thr208=
|
|
NM_030662.4:c.1193C=
MANE Select
|
NP_109587.1:p.Thr398=
|
|