ENST00000394867.9:n.1212T>A
|
|
|
ENST00000687128.1:n.1212T>A
|
|
|
ENST00000688002.1:n.1067T>A
|
|
|
ENST00000689792.1:n.677T>A
|
|
|
ENST00000262948.10:c.773T>A
MANE Select
|
ENSP00000262948.4:p.Val258Glu
|
|
ENST00000262948.9:c.773T>A
|
ENSP00000262948.3:p.Val258Glu
|
|
ENST00000394867.8:c.482T>A
|
ENSP00000378336.1:p.Val161Glu
|
|
ENST00000593364.5:n.720T>A
|
|
|
ENST00000595715.1:n.588T>A
|
|
|
ENST00000597263.5:n.169+1672T>A
|
|
|
ENST00000599021.1:c.29+1672T>A
|
|
|
ENST00000600584.5:n.1333T>A
|
|
|
ENST00000601786.5:n.1074T>A
|
|
|
NM_030662.3:c.773T>A , LRG_750t1:c.773T>A
|
NP_109587.1:p.Val258Glu
|
|
XM_006722799.2:c.705+1672T>A
|
XP_006722862.1:n.705+1672T>A
|
|
XM_011528133.1:c.203T>A
|
XP_011526435.1:p.Val68Glu
|
|
XM_017026989.1:c.773T>A
|
XP_016882478.1:p.Val258Glu
|
|
XM_017026990.1:c.705+1672T>A
|
XP_016882479.1:n.705+1672T>A
|
|
NM_030662.4:c.773T>A
MANE Select
|
NP_109587.1:p.Val258Glu
|
|