ENST00000394867.9:n.1573T>A
|
|
|
ENST00000688002.1:n.3285T>A
|
|
|
ENST00000688751.1:n.270T>A
|
|
|
ENST00000689792.1:n.1038T>A
|
|
|
ENST00000262948.10:c.1134T>A
MANE Select
|
ENSP00000262948.4:p.Asp378Glu
|
|
ENST00000262948.9:c.1134T>A
|
ENSP00000262948.3:p.Asp378Glu
|
|
ENST00000394867.8:c.843T>A
|
ENSP00000378336.1:p.Asp281Glu
|
|
ENST00000597263.5:n.319T>A
|
|
|
ENST00000599021.1:c.244T>A
|
|
|
ENST00000600584.5:n.2583T>A
|
|
|
ENST00000601786.5:n.1435T>A
|
|
|
NM_030662.3:c.1134T>A , LRG_750t1:c.1134T>A
|
NP_109587.1:p.Asp378Glu
|
|
XM_006722799.2:c.855T>A
|
XP_006722862.1:p.Asp285Glu
|
|
XM_011528133.1:c.564T>A
|
XP_011526435.1:p.Asp188Glu
|
|
NM_030662.4:c.1134T>A
MANE Select
|
NP_109587.1:p.Asp378Glu
|
|