|
ENST00000394867.9:n.1581G=
|
|
|
|
ENST00000688002.1:n.3293G=
|
|
|
|
ENST00000688751.1:n.278G=
|
|
|
|
ENST00000689792.1:n.1046G=
|
|
|
|
ENST00000262948.10:c.1142G=
MANE Select
|
ENSP00000262948.4:p.Gly381=
|
|
|
ENST00000262948.9:c.1142G=
|
ENSP00000262948.3:p.Gly381=
|
|
|
ENST00000394867.8:c.851G=
|
ENSP00000378336.1:p.Gly284=
|
|
|
ENST00000597263.5:n.327G=
|
|
|
|
ENST00000599021.1:c.252G=
|
|
|
|
ENST00000600584.5:n.2591G=
|
|
|
|
ENST00000601786.5:n.1443G=
|
|
|
|
NM_030662.3:c.1142G= , LRG_750t1:c.1142G=
|
NP_109587.1:p.Gly381=
|
|
|
XM_006722799.2:c.863G=
|
XP_006722862.1:p.Gly288=
|
|
|
XM_011528133.1:c.572G=
|
XP_011526435.1:p.Gly191=
|
|
|
NM_030662.4:c.1142G=
MANE Select
|
NP_109587.1:p.Gly381=
|
|
