ENST00000394867.9:n.1596C>A
|
|
|
ENST00000688002.1:n.3308C>A
|
|
|
ENST00000688751.1:n.293C>A
|
|
|
ENST00000689792.1:n.1061C>A
|
|
|
ENST00000262948.10:c.1157C>A
MANE Select
|
ENSP00000262948.4:p.Thr386Asn
|
|
ENST00000262948.9:c.1157C>A
|
ENSP00000262948.3:p.Thr386Asn
|
|
ENST00000394867.8:c.866C>A
|
ENSP00000378336.1:p.Thr289Asn
|
|
ENST00000597263.5:n.342C>A
|
|
|
ENST00000599021.1:c.267C>A
|
|
|
ENST00000600584.5:n.2606C>A
|
|
|
ENST00000601786.5:n.1458C>A
|
|
|
NM_030662.3:c.1157C>A , LRG_750t1:c.1157C>A
|
NP_109587.1:p.Thr386Asn
|
|
XM_006722799.2:c.878C>A
|
XP_006722862.1:p.Thr293Asn
|
|
XM_011528133.1:c.587C>A
|
XP_011526435.1:p.Thr196Asn
|
|
NM_030662.4:c.1157C>A
MANE Select
|
NP_109587.1:p.Thr386Asn
|
|