ENST00000695901.1:c.798+767T>C
|
ENSP00000512251.1:n.798+767T>C
|
|
ENST00000695911.1:c.890T>C
|
ENSP00000512262.1:n.890T>C
|
|
ENST00000695912.1:c.1109T>C
|
ENSP00000512263.1:p.Val370Ala
|
|
ENST00000695913.1:c.*1865T>C
|
ENSP00000512264.1:n.*1865T>C
|
|
ENST00000695914.1:c.872T>C
|
ENSP00000512265.1:p.Val291Ala
|
|
ENST00000695918.1:n.340T>C
|
|
|
ENST00000306721.8:c.1112T>C
MANE Select
|
ENSP00000306968.3:p.Val371Ala
|
|
ENST00000306721.7:c.1112T>C
|
ENSP00000306968.3:p.Val371Ala
|
|
ENST00000347703.7:c.875T>C
|
ENSP00000272789.4:p.Val292Ala
|
|
ENST00000410019.3:c.749T>C
|
ENSP00000386833.3:p.Val250Ala
|
|
ENST00000410101.7:c.980T>C
|
ENSP00000386656.3:p.Val327Ala
|
|
ENST00000467411.5:n.1768+767T>C
|
|
|
ENST00000496441.5:n.1866T>C
|
|
|
NM_031942.4:c.1112T>C
|
NP_114148.3:p.Val371Ala
|
|
NM_145810.2:c.875T>C
|
NP_665809.1:p.Val292Ala
|
|
XM_011511957.1:c.1031T>C
|
XP_011510259.1:p.Val344Ala
|
|
XR_923034.1:n.2010T>C
|
|
|
NM_031942.5:c.1112T>C
MANE Select
|
NP_114148.3:p.Val371Ala
|
|
NM_145810.3:c.875T>C
|
NP_665809.1:p.Val292Ala
|
|