ENST00000695901.1:c.798+719A>T
|
ENSP00000512251.1:n.798+719A>T
|
|
ENST00000695911.1:c.842A>T
|
ENSP00000512262.1:n.842A>T
|
|
ENST00000695912.1:c.1061A>T
|
ENSP00000512263.1:p.Lys354Met
|
|
ENST00000695913.1:c.*1817A>T
|
ENSP00000512264.1:n.*1817A>T
|
|
ENST00000695914.1:c.824A>T
|
ENSP00000512265.1:p.Lys275Met
|
|
ENST00000695918.1:n.292A>T
|
|
|
ENST00000306721.8:c.1064A>T
MANE Select
|
ENSP00000306968.3:p.Lys355Met
|
|
ENST00000306721.7:c.1064A>T
|
ENSP00000306968.3:p.Lys355Met
|
|
ENST00000347703.7:c.827A>T
|
ENSP00000272789.4:p.Lys276Met
|
|
ENST00000410019.3:c.701A>T
|
ENSP00000386833.3:p.Lys234Met
|
|
ENST00000410101.7:c.932A>T
|
ENSP00000386656.3:p.Lys311Met
|
|
ENST00000467411.5:n.1768+719A>T
|
|
|
ENST00000496441.5:n.1818A>T
|
|
|
NM_031942.4:c.1064A>T
|
NP_114148.3:p.Lys355Met
|
|
NM_145810.2:c.827A>T
|
NP_665809.1:p.Lys276Met
|
|
XM_011511957.1:c.983A>T
|
XP_011510259.1:p.Lys328Met
|
|
XR_923034.1:n.1962A>T
|
|
|
NM_031942.5:c.1064A>T
MANE Select
|
NP_114148.3:p.Lys355Met
|
|
NM_145810.3:c.827A>T
|
NP_665809.1:p.Lys276Met
|
|