ENST00000695901.1:c.798+755A=
|
ENSP00000512251.1:n.798+755A=
|
|
ENST00000695911.1:c.878A=
|
ENSP00000512262.1:n.878A=
|
|
ENST00000695912.1:c.1097A=
|
ENSP00000512263.1:p.Asp366=
|
|
ENST00000695913.1:c.*1853A=
|
ENSP00000512264.1:n.*1853A=
|
|
ENST00000695914.1:c.860A=
|
ENSP00000512265.1:p.Asp287=
|
|
ENST00000695918.1:n.328A=
|
|
|
ENST00000306721.8:c.1100A=
MANE Select
|
ENSP00000306968.3:p.Asp367=
|
|
ENST00000306721.7:c.1100A=
|
ENSP00000306968.3:p.Asp367=
|
|
ENST00000347703.7:c.863A=
|
ENSP00000272789.4:p.Asp288=
|
|
ENST00000410019.3:c.737A=
|
ENSP00000386833.3:p.Asp246=
|
|
ENST00000410101.7:c.968A=
|
ENSP00000386656.3:p.Asp323=
|
|
ENST00000467411.5:n.1768+755A=
|
|
|
ENST00000496441.5:n.1854A=
|
|
|
NM_031942.4:c.1100A=
|
NP_114148.3:p.Asp367=
|
|
NM_145810.2:c.863A=
|
NP_665809.1:p.Asp288=
|
|
XM_011511957.1:c.1019A=
|
XP_011510259.1:p.Asp340=
|
|
XR_923034.1:n.1998A=
|
|
|
NM_031942.5:c.1100A=
MANE Select
|
NP_114148.3:p.Asp367=
|
|
NM_145810.3:c.863A=
|
NP_665809.1:p.Asp288=
|
|