|
ENST00000394867.9:n.1623C=
|
|
|
|
ENST00000688002.1:n.3335C=
|
|
|
|
ENST00000688751.1:n.320C=
|
|
|
|
ENST00000689792.1:n.1088C=
|
|
|
|
ENST00000262948.10:c.1184C=
MANE Select
|
ENSP00000262948.4:p.Pro395=
|
|
|
ENST00000262948.9:c.1184C=
|
ENSP00000262948.3:p.Pro395=
|
|
|
ENST00000394867.8:c.893C=
|
ENSP00000378336.1:p.Pro298=
|
|
|
ENST00000597263.5:n.369C=
|
|
|
|
ENST00000599021.1:c.294C=
|
|
|
|
ENST00000600584.5:n.2633C=
|
|
|
|
ENST00000601786.5:n.1485C=
|
|
|
|
NM_030662.3:c.1184C= , LRG_750t1:c.1184C=
|
NP_109587.1:p.Pro395=
|
|
|
XM_006722799.2:c.905C=
|
XP_006722862.1:p.Pro302=
|
|
|
XM_011528133.1:c.614C=
|
XP_011526435.1:p.Pro205=
|
|
|
NM_030662.4:c.1184C=
MANE Select
|
NP_109587.1:p.Pro395=
|
|
