ENST00000219548.9:c.534A>C
(STUB1)
MANE Select
|
ENSP00000219548.4:p.Glu178Asp
|
|
ENST00000609261.6:c.*992T>G
(JMJD8)
MANE Select
|
ENSP00000477481.1:n.*992T>G
|
|
ENST00000219548.8:c.534A>C
(STUB1)
|
ENSP00000219548.4:p.Glu178Asp
|
|
ENST00000412368.6:c.*992T>G
(JMJD8)
|
ENSP00000399475.2:n.*992T>G
|
|
ENST00000563505.5:n.630A>C
(STUB1)
|
|
|
ENST00000564316.1:c.133A>C
(STUB1)
|
|
|
ENST00000564370.5:c.318A>C
(STUB1)
|
ENSP00000456875.1:p.Glu106Asp
|
|
ENST00000565302.5:n.1871T>G
(JMJD8)
|
|
|
ENST00000565677.5:c.318A>C
(STUB1)
|
ENSP00000457228.1:p.Glu106Asp
|
|
ENST00000566181.2:n.303A>C
(STUB1)
|
|
|
ENST00000566408.5:c.251A>C
(STUB1)
|
|
|
ENST00000567120.5:n.2074T>G
(JMJD8)
|
|
|
ENST00000567173.5:c.477A>C
(STUB1)
|
ENSP00000456591.1:p.Glu159Asp
|
|
ENST00000568689.5:n.1895T>G
(JMJD8)
|
|
|
ENST00000569248.5:n.1108A>C
(STUB1)
|
|
|
ENST00000609261.5:c.*992T>G
(JMJD8)
|
ENSP00000477481.1:n.*992T>G
|
|
ENST00000620831.4:c.-50+38499A>C
(MSLN)
|
ENSP00000482893.1:n.-50+38499A>C
|
|
NM_001005920.2:c.*992T>G
(JMJD8)
|
NP_001005920.2:n.*992T>G
|
|
NM_001293197.1:c.318A>C
(STUB1)
|
NP_001280126.1:p.Glu106Asp
|
|
NM_005861.3:c.534A>C
(STUB1)
|
NP_005852.2:p.Glu178Asp
|
|
XM_005255295.3:c.*1026T>G
(JMJD8)
|
XP_005255352.1:n.*1026T>G
|
|
XM_005255297.3:c.*992T>G
(JMJD8)
|
XP_005255354.1:n.*992T>G
|
|
XM_011522474.1:c.*992T>G
(JMJD8)
|
XP_011520776.1:n.*992T>G
|
|
NM_001005920.3:c.*992T>G
(JMJD8)
|
NP_001005920.3:n.*992T>G
|
|
NM_001323918.2:c.*1026T>G
(JMJD8)
|
NP_001310847.2:n.*1026T>G
|
|
NM_001323919.2:c.*992T>G
(JMJD8)
|
NP_001310848.2:n.*992T>G
|
|
NM_001323920.2:c.*992T>G
(JMJD8)
|
NP_001310849.2:n.*992T>G
|
|
NM_001323922.2:c.*1026T>G
(JMJD8)
|
NP_001310851.2:n.*1026T>G
|
|
NR_136650.2:n.1885T>G
(JMJD8)
|
|
|
NR_136651.2:n.1890T>G
(JMJD8)
|
|
|
NR_136652.2:n.1800T>G
(JMJD8)
|
|
|
NM_001005920.4:c.*992T>G
(JMJD8)
MANE Select
|
NP_001005920.3:n.*992T>G
|
|
NM_005861.4:c.534A>C
(STUB1)
MANE Select
|
NP_005852.2:p.Glu178Asp
|
|
NM_001293197.2:c.318A>C
(STUB1)
|
NP_001280126.1:p.Glu106Asp
|
|
NM_001323918.3:c.*1026T>G
(JMJD8)
|
NP_001310847.2:n.*1026T>G
|
|
NM_001323919.3:c.*992T>G
(JMJD8)
|
NP_001310848.2:n.*992T>G
|
|
NM_001323920.3:c.*992T>G
(JMJD8)
|
NP_001310849.2:n.*992T>G
|
|
NM_001323922.3:c.*1026T>G
(JMJD8)
|
NP_001310851.2:n.*1026T>G
|
|
NR_136650.3:n.1885T>G
(JMJD8)
|
|
|
NR_136651.3:n.1890T>G
(JMJD8)
|
|
|
NR_136652.3:n.1800T>G
(JMJD8)
|
|
|