ENST00000449682.3:c.*57G>T
(MST1)
MANE Select
|
ENSP00000414287.2:n.*57G>T
|
|
ENST00000296456.10:c.*629C>A
(APEH)
MANE Select
|
ENSP00000296456.5:n.*629C>A
|
|
ENST00000448220.5:c.643G>T
(MST1)
|
|
|
ENST00000449682.2:c.*57G>T
(MST1)
|
ENSP00000414287.2:n.*57G>T
|
|
NM_020998.3:c.*57G>T
(MST1)
|
NP_066278.3:n.*57G>T
|
|
XM_006713166.1:c.*57G>T
(MST1)
|
XP_006713229.1:n.*57G>T
|
|
XM_011533730.1:c.*57G>T
(MST1)
|
XP_011532032.1:n.*57G>T
|
|
XM_011533731.1:c.*57G>T
(MST1)
|
XP_011532033.1:n.*57G>T
|
|
XM_011533732.1:c.*57G>T
(MST1)
|
XP_011532034.1:n.*57G>T
|
|
XM_011533733.1:c.*155G>T
(MST1)
|
XP_011532035.1:n.*155G>T
|
|
XR_427270.2:n.3167G>T
(MST1)
|
|
|
XR_427271.1:n.3118G>T
(MST1)
|
|
|
XR_427273.1:n.3023G>T
(MST1)
|
|
|
XR_427274.2:n.3068G>T
(MST1)
|
|
|
XR_940425.1:n.3163G>T
(MST1)
|
|
|
XR_940426.1:n.3203G>T
(MST1)
|
|
|
XR_940427.1:n.3068G>T
(MST1)
|
|
|
NR_146060.1:n.2188G>T
(MST1)
|
|
|
XM_006713166.2:c.*57G>T
(MST1)
|
XP_006713229.1:n.*57G>T
|
|
XM_011533732.2:c.*57G>T
(MST1)
|
XP_011532034.1:n.*57G>T
|
|
XM_017006460.2:c.*57G>T
(MST1)
|
XP_016861949.1:n.*57G>T
|
|
XM_017006461.2:c.*57G>T
(MST1)
|
XP_016861950.1:n.*57G>T
|
|
XM_017006462.2:c.*155G>T
(MST1)
|
XP_016861951.1:n.*155G>T
|
|
XM_017006463.2:c.*155G>T
(MST1)
|
XP_016861952.1:n.*155G>T
|
|
XM_017006464.2:c.*155G>T
(MST1)
|
XP_016861953.1:n.*155G>T
|
|
XR_001740149.2:n.2335G>T
(MST1)
|
|
|
XR_001740150.2:n.2332G>T
(MST1)
|
|
|
XR_001740151.2:n.2375G>T
(MST1)
|
|
|
XR_001740152.2:n.2290G>T
(MST1)
|
|
|
XR_001740153.2:n.2336G>T
(MST1)
|
|
|
XR_002959536.1:n.2290G>T
(MST1)
|
|
|
XR_427273.2:n.2294G>T
(MST1)
|
|
|
XR_940427.2:n.2339G>T
(MST1)
|
|
|
NM_001640.4:c.*629C>A
(APEH)
MANE Select
|
NP_001631.3:n.*629C>A
|
|
NM_001393581.1:c.*57G>T
(MST1)
|
NP_001380510.1:n.*57G>T
|
|
NM_001393582.1:c.*57G>T
(MST1)
|
NP_001380511.1:n.*57G>T
|
|
NM_001393583.1:c.*57G>T
(MST1)
|
NP_001380512.1:n.*57G>T
|
|
NM_001393584.1:c.*57G>T
(MST1)
|
NP_001380513.1:n.*57G>T
|
|
NM_001393585.1:c.*57G>T
(MST1)
|
NP_001380514.1:n.*57G>T
|
|
NM_020998.4:c.*57G>T
(MST1)
MANE Select
|
NP_066278.3:n.*57G>T
|
|
NR_146060.2:n.2899G>T
(MST1)
|
|
|