ENST00000394867.9:n.1498C>T
|
|
|
ENST00000688002.1:n.3210C>T
|
|
|
ENST00000688751.1:n.195C>T
|
|
|
ENST00000689792.1:n.963C>T
|
|
|
ENST00000262948.10:c.1059C>T
MANE Select
|
ENSP00000262948.4:p.Asn353=
|
|
ENST00000262948.9:c.1059C>T
|
ENSP00000262948.3:p.Asn353=
|
|
ENST00000394867.8:c.768C>T
|
ENSP00000378336.1:p.Asn256=
|
|
ENST00000597263.5:n.244C>T
|
|
|
ENST00000599021.1:c.169C>T
|
|
|
ENST00000600584.5:n.2508C>T
|
|
|
ENST00000601786.5:n.1360C>T
|
|
|
NM_030662.3:c.1059C>T , LRG_750t1:c.1059C>T
|
NP_109587.1:p.Asn353=
|
|
XM_006722799.2:c.780C>T
|
XP_006722862.1:p.Asn260=
|
|
XM_011528133.1:c.489C>T
|
XP_011526435.1:p.Asn163=
|
|
NM_030662.4:c.1059C>T
MANE Select
|
NP_109587.1:p.Asn353=
|
|