|
ENST00000394867.9:n.1598C=
|
|
|
|
ENST00000688002.1:n.3310C=
|
|
|
|
ENST00000688751.1:n.295C=
|
|
|
|
ENST00000689792.1:n.1063C=
|
|
|
|
ENST00000262948.10:c.1159C=
MANE Select
|
ENSP00000262948.4:p.Leu387=
|
|
|
ENST00000262948.9:c.1159C=
|
ENSP00000262948.3:p.Leu387=
|
|
|
ENST00000394867.8:c.868C=
|
ENSP00000378336.1:p.Leu290=
|
|
|
ENST00000597263.5:n.344C=
|
|
|
|
ENST00000599021.1:c.269C=
|
|
|
|
ENST00000600584.5:n.2608C=
|
|
|
|
ENST00000601786.5:n.1460C=
|
|
|
|
NM_030662.3:c.1159C= , LRG_750t1:c.1159C=
|
NP_109587.1:p.Leu387=
|
|
|
XM_006722799.2:c.880C=
|
XP_006722862.1:p.Leu294=
|
|
|
XM_011528133.1:c.589C=
|
XP_011526435.1:p.Leu197=
|
|
|
NM_030662.4:c.1159C=
MANE Select
|
NP_109587.1:p.Leu387=
|
|
