ENST00000394867.9:n.1633C=
|
|
|
ENST00000688002.1:n.3345C=
|
|
|
ENST00000688751.1:n.330C=
|
|
|
ENST00000689792.1:n.1098C=
|
|
|
ENST00000262948.10:c.1194C=
MANE Select
|
ENSP00000262948.4:p.Thr398=
|
|
ENST00000262948.9:c.1194C=
|
ENSP00000262948.3:p.Thr398=
|
|
ENST00000394867.8:c.903C=
|
ENSP00000378336.1:p.Thr301=
|
|
ENST00000597263.5:n.379C=
|
|
|
ENST00000599021.1:c.304C=
|
|
|
ENST00000600584.5:n.2643C=
|
|
|
ENST00000601786.5:n.1495C=
|
|
|
NM_030662.3:c.1194C= , LRG_750t1:c.1194C=
|
NP_109587.1:p.Thr398=
|
|
XM_006722799.2:c.915C=
|
XP_006722862.1:p.Thr305=
|
|
XM_011528133.1:c.624C=
|
XP_011526435.1:p.Thr208=
|
|
NM_030662.4:c.1194C=
MANE Select
|
NP_109587.1:p.Thr398=
|
|