ENST00000695651.1:n.876A>T
|
|
|
ENST00000695652.1:c.2405A>T
|
ENSP00000512083.1:p.Glu802Val
|
|
ENST00000695653.1:c.437A>T
|
ENSP00000512084.1:p.Glu146Val
|
|
ENST00000695654.1:c.1652A>T
|
ENSP00000512085.1:p.Glu551Val
|
|
ENST00000695655.1:c.1469A>T
|
ENSP00000512086.1:n.1469A>T
|
|
ENST00000695692.1:n.1892A>T
|
|
|
ENST00000245907.11:c.2528A>T
MANE Select
|
ENSP00000245907.4:p.Glu843Val
|
|
ENST00000245907.10:c.2528A>T
|
ENSP00000245907.4:p.Glu843Val
|
|
ENST00000594005.1:n.9A>T
|
|
|
ENST00000602053.1:n.576A>T
|
|
|
NM_000064.3:c.2528A>T
|
NP_000055.2:p.Glu843Val
|
|
NM_000064.4:c.2528A>T
MANE Select
|
NP_000055.2:p.Glu843Val
|
|