ENST00000449682.3:c.2176T>A
MANE Select
|
ENSP00000414287.2:p.Ter726Lys
|
|
ENST00000448220.5:c.584T>A
|
|
|
ENST00000449682.2:c.2176T>A
|
ENSP00000414287.2:p.Ter726Lys
|
|
ENST00000479115.5:n.2231T>A
|
|
|
ENST00000488350.6:n.4098T>A
|
|
|
ENST00000492329.5:n.1952T>A
|
|
|
NM_020998.3:c.2176T>A
|
NP_066278.3:p.Ter726Lys
|
|
XM_006713166.1:c.2041T>A
|
XP_006713229.1:p.Ter681Lys
|
|
XM_011533730.1:c.2311T>A
|
XP_011532032.1:p.Ter771Lys
|
|
XM_011533731.1:c.2218T>A
|
XP_011532033.1:p.Ter740Lys
|
|
XM_011533732.1:c.2212T>A
|
XP_011532034.1:p.Ter738Lys
|
|
XM_011533733.1:c.*96T>A
|
XP_011532035.1:n.*96T>A
|
|
XR_427270.2:n.3108T>A
|
|
|
XR_427271.1:n.3059T>A
|
|
|
XR_427273.1:n.2964T>A
|
|
|
XR_427274.2:n.3009T>A
|
|
|
XR_940425.1:n.3104T>A
|
|
|
XR_940426.1:n.3144T>A
|
|
|
XR_940427.1:n.3009T>A
|
|
|
NR_146060.1:n.2129T>A
|
|
|
XM_006713166.2:c.2041T>A
|
XP_006713229.1:p.Ter681Lys
|
|
XM_011533732.2:c.2212T>A
|
XP_011532034.1:p.Ter738Lys
|
|
XM_017006460.2:c.2155T>A
|
XP_016861949.1:p.Ter719Lys
|
|
XM_017006461.2:c.2119T>A
|
XP_016861950.1:p.Ter707Lys
|
|
XM_017006462.2:c.*96T>A
|
XP_016861951.1:n.*96T>A
|
|
XM_017006463.2:c.*96T>A
|
XP_016861952.1:n.*96T>A
|
|
XM_017006464.2:c.*96T>A
|
XP_016861953.1:n.*96T>A
|
|
XR_001740149.2:n.2276T>A
|
|
|
XR_001740150.2:n.2273T>A
|
|
|
XR_001740151.2:n.2316T>A
|
|
|
XR_001740152.2:n.2231T>A
|
|
|
XR_001740153.2:n.2277T>A
|
|
|
XR_002959536.1:n.2231T>A
|
|
|
XR_427273.2:n.2235T>A
|
|
|
XR_940427.2:n.2280T>A
|
|
|
NM_001393581.1:c.2212T>A
|
NP_001380510.1:p.Ter738Lys
|
|
NM_001393582.1:c.2119T>A
|
NP_001380511.1:p.Ter707Lys
|
|
NM_001393583.1:c.2086T>A
|
NP_001380512.1:p.Ter696Lys
|
|
NM_001393584.1:c.2041T>A
|
NP_001380513.1:p.Ter681Lys
|
|
NM_001393585.1:c.1876T>A
|
NP_001380514.1:p.Ter626Lys
|
|
NM_020998.4:c.2176T>A
MANE Select
|
NP_066278.3:p.Ter726Lys
|
|
NR_146060.2:n.2840T>A
|
|
|