ENST00000695901.1:c.798+766G>A
|
ENSP00000512251.1:n.798+766G>A
|
|
ENST00000695911.1:c.889G>A
|
ENSP00000512262.1:n.889G>A
|
|
ENST00000695912.1:c.1108G>A
|
ENSP00000512263.1:p.Val370Ile
|
|
ENST00000695913.1:c.*1864G>A
|
ENSP00000512264.1:n.*1864G>A
|
|
ENST00000695914.1:c.871G>A
|
ENSP00000512265.1:p.Val291Ile
|
|
ENST00000695918.1:n.339G>A
|
|
|
ENST00000306721.8:c.1111G>A
MANE Select
|
ENSP00000306968.3:p.Val371Ile
|
|
ENST00000306721.7:c.1111G>A
|
ENSP00000306968.3:p.Val371Ile
|
|
ENST00000347703.7:c.874G>A
|
ENSP00000272789.4:p.Val292Ile
|
|
ENST00000410019.3:c.748G>A
|
ENSP00000386833.3:p.Val250Ile
|
|
ENST00000410101.7:c.979G>A
|
ENSP00000386656.3:p.Val327Ile
|
|
ENST00000467411.5:n.1768+766G>A
|
|
|
ENST00000496441.5:n.1865G>A
|
|
|
NM_031942.4:c.1111G>A
|
NP_114148.3:p.Val371Ile
|
|
NM_145810.2:c.874G>A
|
NP_665809.1:p.Val292Ile
|
|
XM_011511957.1:c.1030G>A
|
XP_011510259.1:p.Val344Ile
|
|
XR_923034.1:n.2009G>A
|
|
|
NM_031942.5:c.1111G>A
MANE Select
|
NP_114148.3:p.Val371Ile
|
|
NM_145810.3:c.874G>A
|
NP_665809.1:p.Val292Ile
|
|