|
ENST00000394867.9:n.1589T=
|
|
|
|
ENST00000688002.1:n.3301T=
|
|
|
|
ENST00000688751.1:n.286T=
|
|
|
|
ENST00000689792.1:n.1054T=
|
|
|
|
ENST00000262948.10:c.1150T=
MANE Select
|
ENSP00000262948.4:p.Cys384=
|
|
|
ENST00000262948.9:c.1150T=
|
ENSP00000262948.3:p.Cys384=
|
|
|
ENST00000394867.8:c.859T=
|
ENSP00000378336.1:p.Cys287=
|
|
|
ENST00000597263.5:n.335T=
|
|
|
|
ENST00000599021.1:c.260T=
|
|
|
|
ENST00000600584.5:n.2599T=
|
|
|
|
ENST00000601786.5:n.1451T=
|
|
|
|
NM_030662.3:c.1150T= , LRG_750t1:c.1150T=
|
NP_109587.1:p.Cys384=
|
|
|
XM_006722799.2:c.871T=
|
XP_006722862.1:p.Cys291=
|
|
|
XM_011528133.1:c.580T=
|
XP_011526435.1:p.Cys194=
|
|
|
NM_030662.4:c.1150T=
MANE Select
|
NP_109587.1:p.Cys384=
|
|
