ENST00000394867.9:n.1591T>A
|
|
|
ENST00000688002.1:n.3303T>A
|
|
|
ENST00000688751.1:n.288T>A
|
|
|
ENST00000689792.1:n.1056T>A
|
|
|
ENST00000262948.10:c.1152T>A
MANE Select
|
ENSP00000262948.4:p.Cys384Ter
|
|
ENST00000262948.9:c.1152T>A
|
ENSP00000262948.3:p.Cys384Ter
|
|
ENST00000394867.8:c.861T>A
|
ENSP00000378336.1:p.Cys287Ter
|
|
ENST00000597263.5:n.337T>A
|
|
|
ENST00000599021.1:c.262T>A
|
|
|
ENST00000600584.5:n.2601T>A
|
|
|
ENST00000601786.5:n.1453T>A
|
|
|
NM_030662.3:c.1152T>A , LRG_750t1:c.1152T>A
|
NP_109587.1:p.Cys384Ter
|
|
XM_006722799.2:c.873T>A
|
XP_006722862.1:p.Cys291Ter
|
|
XM_011528133.1:c.582T>A
|
XP_011526435.1:p.Cys194Ter
|
|
NM_030662.4:c.1152T>A
MANE Select
|
NP_109587.1:p.Cys384Ter
|
|