ENST00000394867.9:n.1556G>T
|
|
|
ENST00000688002.1:n.3268G>T
|
|
|
ENST00000688751.1:n.253G>T
|
|
|
ENST00000689792.1:n.1021G>T
|
|
|
ENST00000262948.10:c.1117G>T
MANE Select
|
ENSP00000262948.4:p.Glu373Ter
|
|
ENST00000262948.9:c.1117G>T
|
ENSP00000262948.3:p.Glu373Ter
|
|
ENST00000394867.8:c.826G>T
|
ENSP00000378336.1:p.Glu276Ter
|
|
ENST00000597263.5:n.302G>T
|
|
|
ENST00000599021.1:c.227G>T
|
|
|
ENST00000600584.5:n.2566G>T
|
|
|
ENST00000601786.5:n.1418G>T
|
|
|
NM_030662.3:c.1117G>T , LRG_750t1:c.1117G>T
|
NP_109587.1:p.Glu373Ter
|
|
XM_006722799.2:c.838G>T
|
XP_006722862.1:p.Glu280Ter
|
|
XM_011528133.1:c.547G>T
|
XP_011526435.1:p.Glu183Ter
|
|
NM_030662.4:c.1117G>T
MANE Select
|
NP_109587.1:p.Glu373Ter
|
|