ENST00000394867.9:n.1468G>A
|
|
|
ENST00000688002.1:n.3180G>A
|
|
|
ENST00000688751.1:n.165G>A
|
|
|
ENST00000689792.1:n.933G>A
|
|
|
ENST00000262948.10:c.1029G>A
MANE Select
|
ENSP00000262948.4:p.Gln343=
|
|
ENST00000262948.9:c.1029G>A
|
ENSP00000262948.3:p.Gln343=
|
|
ENST00000394867.8:c.738G>A
|
ENSP00000378336.1:p.Gln246=
|
|
ENST00000595715.1:n.844G>A
|
|
|
ENST00000597263.5:n.214G>A
|
|
|
ENST00000599021.1:c.139G>A
|
|
|
ENST00000600584.5:n.1589G>A
|
|
|
ENST00000601786.5:n.1330G>A
|
|
|
NM_030662.3:c.1029G>A , LRG_750t1:c.1029G>A
|
NP_109587.1:p.Gln343=
|
|
XM_006722799.2:c.750G>A
|
XP_006722862.1:p.Gln250=
|
|
XM_011528133.1:c.459G>A
|
XP_011526435.1:p.Gln153=
|
|
XM_017026989.1:c.1029G>A
|
XP_016882478.1:p.Gln343=
|
|
XM_017026990.1:c.750G>A
|
XP_016882479.1:p.Gln250=
|
|
NM_030662.4:c.1029G>A
MANE Select
|
NP_109587.1:p.Gln343=
|
|