ENST00000394867.9:n.1597C>G
|
|
|
ENST00000688002.1:n.3309C>G
|
|
|
ENST00000688751.1:n.294C>G
|
|
|
ENST00000689792.1:n.1062C>G
|
|
|
ENST00000262948.10:c.1158C>G
MANE Select
|
ENSP00000262948.4:p.Thr386=
|
|
ENST00000262948.9:c.1158C>G
|
ENSP00000262948.3:p.Thr386=
|
|
ENST00000394867.8:c.867C>G
|
ENSP00000378336.1:p.Thr289=
|
|
ENST00000597263.5:n.343C>G
|
|
|
ENST00000599021.1:c.268C>G
|
|
|
ENST00000600584.5:n.2607C>G
|
|
|
ENST00000601786.5:n.1459C>G
|
|
|
NM_030662.3:c.1158C>G , LRG_750t1:c.1158C>G
|
NP_109587.1:p.Thr386=
|
|
XM_006722799.2:c.879C>G
|
XP_006722862.1:p.Thr293=
|
|
XM_011528133.1:c.588C>G
|
XP_011526435.1:p.Thr196=
|
|
NM_030662.4:c.1158C>G
MANE Select
|
NP_109587.1:p.Thr386=
|
|