ENST00000695651.1:n.2040A>T
|
|
|
ENST00000695652.1:c.3569A>T
|
ENSP00000512083.1:p.Glu1190Val
|
|
ENST00000695653.1:c.1601A>T
|
ENSP00000512084.1:p.Glu534Val
|
|
ENST00000695654.1:c.2717A>T
|
ENSP00000512085.1:p.Glu906Val
|
|
ENST00000695655.1:c.2633A>T
|
ENSP00000512086.1:n.2633A>T
|
|
ENST00000695692.1:n.3056A>T
|
|
|
ENST00000245907.11:c.3692A>T
MANE Select
|
ENSP00000245907.4:p.Glu1231Val
|
|
ENST00000245907.10:c.3692A>T
|
ENSP00000245907.4:p.Glu1231Val
|
|
ENST00000596238.1:n.135A>T
|
|
|
ENST00000601008.1:c.241+504A>T
|
ENSP00000471384.1:n.241+504A>T
|
|
NM_000064.3:c.3692A>T
|
NP_000055.2:p.Glu1231Val
|
|
NM_000064.4:c.3692A>T
MANE Select
|
NP_000055.2:p.Glu1231Val
|
|