ENST00000449682.3:c.*59C>T
(MST1)
MANE Select
|
ENSP00000414287.2:n.*59C>T
|
|
ENST00000296456.10:c.*627G>A
(APEH)
MANE Select
|
ENSP00000296456.5:n.*627G>A
|
|
ENST00000448220.5:c.645C>T
(MST1)
|
|
|
ENST00000449682.2:c.*59C>T
(MST1)
|
ENSP00000414287.2:n.*59C>T
|
|
NM_020998.3:c.*59C>T
(MST1)
|
NP_066278.3:n.*59C>T
|
|
XM_006713166.1:c.*59C>T
(MST1)
|
XP_006713229.1:n.*59C>T
|
|
XM_011533730.1:c.*59C>T
(MST1)
|
XP_011532032.1:n.*59C>T
|
|
XM_011533731.1:c.*59C>T
(MST1)
|
XP_011532033.1:n.*59C>T
|
|
XM_011533732.1:c.*59C>T
(MST1)
|
XP_011532034.1:n.*59C>T
|
|
XM_011533733.1:c.*157C>T
(MST1)
|
XP_011532035.1:n.*157C>T
|
|
XR_427270.2:n.3169C>T
(MST1)
|
|
|
XR_427271.1:n.3120C>T
(MST1)
|
|
|
XR_427273.1:n.3025C>T
(MST1)
|
|
|
XR_427274.2:n.3070C>T
(MST1)
|
|
|
XR_940425.1:n.3165C>T
(MST1)
|
|
|
XR_940426.1:n.3205C>T
(MST1)
|
|
|
XR_940427.1:n.3070C>T
(MST1)
|
|
|
NR_146060.1:n.2190C>T
(MST1)
|
|
|
XM_006713166.2:c.*59C>T
(MST1)
|
XP_006713229.1:n.*59C>T
|
|
XM_011533732.2:c.*59C>T
(MST1)
|
XP_011532034.1:n.*59C>T
|
|
XM_017006460.2:c.*59C>T
(MST1)
|
XP_016861949.1:n.*59C>T
|
|
XM_017006461.2:c.*59C>T
(MST1)
|
XP_016861950.1:n.*59C>T
|
|
XM_017006462.2:c.*157C>T
(MST1)
|
XP_016861951.1:n.*157C>T
|
|
XM_017006463.2:c.*157C>T
(MST1)
|
XP_016861952.1:n.*157C>T
|
|
XM_017006464.2:c.*157C>T
(MST1)
|
XP_016861953.1:n.*157C>T
|
|
XR_001740149.2:n.2337C>T
(MST1)
|
|
|
XR_001740150.2:n.2334C>T
(MST1)
|
|
|
XR_001740151.2:n.2377C>T
(MST1)
|
|
|
XR_001740152.2:n.2292C>T
(MST1)
|
|
|
XR_001740153.2:n.2338C>T
(MST1)
|
|
|
XR_002959536.1:n.2292C>T
(MST1)
|
|
|
XR_427273.2:n.2296C>T
(MST1)
|
|
|
XR_940427.2:n.2341C>T
(MST1)
|
|
|
NM_001640.4:c.*627G>A
(APEH)
MANE Select
|
NP_001631.3:n.*627G>A
|
|
NM_001393581.1:c.*59C>T
(MST1)
|
NP_001380510.1:n.*59C>T
|
|
NM_001393582.1:c.*59C>T
(MST1)
|
NP_001380511.1:n.*59C>T
|
|
NM_001393583.1:c.*59C>T
(MST1)
|
NP_001380512.1:n.*59C>T
|
|
NM_001393584.1:c.*59C>T
(MST1)
|
NP_001380513.1:n.*59C>T
|
|
NM_001393585.1:c.*59C>T
(MST1)
|
NP_001380514.1:n.*59C>T
|
|
NM_020998.4:c.*59C>T
(MST1)
MANE Select
|
NP_066278.3:n.*59C>T
|
|
NR_146060.2:n.2901C>T
(MST1)
|
|
|