ENST00000695651.1:n.814G>T
|
|
|
ENST00000695652.1:c.2343G>T
|
ENSP00000512083.1:p.Glu781Asp
|
|
ENST00000695653.1:c.375G>T
|
ENSP00000512084.1:p.Glu125Asp
|
|
ENST00000695654.1:c.1590G>T
|
ENSP00000512085.1:p.Glu530Asp
|
|
ENST00000695655.1:c.1407G>T
|
ENSP00000512086.1:n.1407G>T
|
|
ENST00000695692.1:n.1830G>T
|
|
|
ENST00000245907.11:c.2466G>T
MANE Select
|
ENSP00000245907.4:p.Glu822Asp
|
|
ENST00000245907.10:c.2466G>T
|
ENSP00000245907.4:p.Glu822Asp
|
|
ENST00000602053.1:n.514G>T
|
|
|
NM_000064.3:c.2466G>T
|
NP_000055.2:p.Glu822Asp
|
|
NM_000064.4:c.2466G>T
MANE Select
|
NP_000055.2:p.Glu822Asp
|
|