ENST00000695901.1:c.798+718A>T
|
ENSP00000512251.1:n.798+718A>T
|
|
ENST00000695911.1:c.841A>T
|
ENSP00000512262.1:n.841A>T
|
|
ENST00000695912.1:c.1060A>T
|
ENSP00000512263.1:p.Lys354Ter
|
|
ENST00000695913.1:c.*1816A>T
|
ENSP00000512264.1:n.*1816A>T
|
|
ENST00000695914.1:c.823A>T
|
ENSP00000512265.1:p.Lys275Ter
|
|
ENST00000695918.1:n.291A>T
|
|
|
ENST00000306721.8:c.1063A>T
MANE Select
|
ENSP00000306968.3:p.Lys355Ter
|
|
ENST00000306721.7:c.1063A>T
|
ENSP00000306968.3:p.Lys355Ter
|
|
ENST00000347703.7:c.826A>T
|
ENSP00000272789.4:p.Lys276Ter
|
|
ENST00000410019.3:c.700A>T
|
ENSP00000386833.3:p.Lys234Ter
|
|
ENST00000410101.7:c.931A>T
|
ENSP00000386656.3:p.Lys311Ter
|
|
ENST00000467411.5:n.1768+718A>T
|
|
|
ENST00000496441.5:n.1817A>T
|
|
|
NM_031942.4:c.1063A>T
|
NP_114148.3:p.Lys355Ter
|
|
NM_145810.2:c.826A>T
|
NP_665809.1:p.Lys276Ter
|
|
XM_011511957.1:c.982A>T
|
XP_011510259.1:p.Lys328Ter
|
|
XR_923034.1:n.1961A>T
|
|
|
NM_031942.5:c.1063A>T
MANE Select
|
NP_114148.3:p.Lys355Ter
|
|
NM_145810.3:c.826A>T
|
NP_665809.1:p.Lys276Ter
|
|