ENST00000394867.9:n.1493A>T
|
|
|
ENST00000688002.1:n.3205A>T
|
|
|
ENST00000688751.1:n.190A>T
|
|
|
ENST00000689792.1:n.958A>T
|
|
|
ENST00000262948.10:c.1054A>T
MANE Select
|
ENSP00000262948.4:p.Lys352Ter
|
|
ENST00000262948.9:c.1054A>T
|
ENSP00000262948.3:p.Lys352Ter
|
|
ENST00000394867.8:c.763A>T
|
ENSP00000378336.1:p.Lys255Ter
|
|
ENST00000597263.5:n.239A>T
|
|
|
ENST00000599021.1:c.164A>T
|
|
|
ENST00000600584.5:n.2503A>T
|
|
|
ENST00000601786.5:n.1355A>T
|
|
|
NM_030662.3:c.1054A>T , LRG_750t1:c.1054A>T
|
NP_109587.1:p.Lys352Ter
|
|
XM_006722799.2:c.775A>T
|
XP_006722862.1:p.Lys259Ter
|
|
XM_011528133.1:c.484A>T
|
XP_011526435.1:p.Lys162Ter
|
|
NM_030662.4:c.1054A>T
MANE Select
|
NP_109587.1:p.Lys352Ter
|
|