ENST00000449682.3:c.2178G>T
MANE Select
|
ENSP00000414287.2:p.Ter726Tyr
|
|
ENST00000448220.5:c.586G>T
|
|
|
ENST00000449682.2:c.2178G>T
|
ENSP00000414287.2:p.Ter726Tyr
|
|
ENST00000479115.5:n.2233G>T
|
|
|
ENST00000488350.6:n.4100G>T
|
|
|
ENST00000492329.5:n.1954G>T
|
|
|
NM_020998.3:c.2178G>T
|
NP_066278.3:p.Ter726Tyr
|
|
XM_006713166.1:c.2043G>T
|
XP_006713229.1:p.Ter681Tyr
|
|
XM_011533730.1:c.2313G>T
|
XP_011532032.1:p.Ter771Tyr
|
|
XM_011533731.1:c.2220G>T
|
XP_011532033.1:p.Ter740Tyr
|
|
XM_011533732.1:c.2214G>T
|
XP_011532034.1:p.Ter738Tyr
|
|
XM_011533733.1:c.*98G>T
|
XP_011532035.1:n.*98G>T
|
|
XR_427270.2:n.3110G>T
|
|
|
XR_427271.1:n.3061G>T
|
|
|
XR_427273.1:n.2966G>T
|
|
|
XR_427274.2:n.3011G>T
|
|
|
XR_940425.1:n.3106G>T
|
|
|
XR_940426.1:n.3146G>T
|
|
|
XR_940427.1:n.3011G>T
|
|
|
NR_146060.1:n.2131G>T
|
|
|
XM_006713166.2:c.2043G>T
|
XP_006713229.1:p.Ter681Tyr
|
|
XM_011533732.2:c.2214G>T
|
XP_011532034.1:p.Ter738Tyr
|
|
XM_017006460.2:c.2157G>T
|
XP_016861949.1:p.Ter719Tyr
|
|
XM_017006461.2:c.2121G>T
|
XP_016861950.1:p.Ter707Tyr
|
|
XM_017006462.2:c.*98G>T
|
XP_016861951.1:n.*98G>T
|
|
XM_017006463.2:c.*98G>T
|
XP_016861952.1:n.*98G>T
|
|
XM_017006464.2:c.*98G>T
|
XP_016861953.1:n.*98G>T
|
|
XR_001740149.2:n.2278G>T
|
|
|
XR_001740150.2:n.2275G>T
|
|
|
XR_001740151.2:n.2318G>T
|
|
|
XR_001740152.2:n.2233G>T
|
|
|
XR_001740153.2:n.2279G>T
|
|
|
XR_002959536.1:n.2233G>T
|
|
|
XR_427273.2:n.2237G>T
|
|
|
XR_940427.2:n.2282G>T
|
|
|
NM_001393581.1:c.2214G>T
|
NP_001380510.1:p.Ter738Tyr
|
|
NM_001393582.1:c.2121G>T
|
NP_001380511.1:p.Ter707Tyr
|
|
NM_001393583.1:c.2088G>T
|
NP_001380512.1:p.Ter696Tyr
|
|
NM_001393584.1:c.2043G>T
|
NP_001380513.1:p.Ter681Tyr
|
|
NM_001393585.1:c.1878G>T
|
NP_001380514.1:p.Ter626Tyr
|
|
NM_020998.4:c.2178G>T
MANE Select
|
NP_066278.3:p.Ter726Tyr
|
|
NR_146060.2:n.2842G>T
|
|
|