|
ENST00000219548.9:c.549C>A
(STUB1)
MANE Select
|
ENSP00000219548.4:p.Asn183Lys
|
|
|
ENST00000609261.6:c.*977G>T
(JMJD8)
MANE Select
|
ENSP00000477481.1:n.*977G>T
|
|
|
ENST00000219548.8:c.549C>A
(STUB1)
|
ENSP00000219548.4:p.Asn183Lys
|
|
|
ENST00000412368.6:c.*977G>T
(JMJD8)
|
ENSP00000399475.2:n.*977G>T
|
|
|
ENST00000563505.5:n.645C>A
(STUB1)
|
|
|
|
ENST00000564316.1:c.148C>A
(STUB1)
|
|
|
|
ENST00000564370.5:c.333C>A
(STUB1)
|
ENSP00000456875.1:p.Asn111Lys
|
|
|
ENST00000565302.5:n.1856G>T
(JMJD8)
|
|
|
|
ENST00000565677.5:c.333C>A
(STUB1)
|
ENSP00000457228.1:p.Asn111Lys
|
|
|
ENST00000566181.2:n.318C>A
(STUB1)
|
|
|
|
ENST00000566408.5:c.266C>A
(STUB1)
|
|
|
|
ENST00000567120.5:n.2059G>T
(JMJD8)
|
|
|
|
ENST00000567173.5:c.492C>A
(STUB1)
|
ENSP00000456591.1:p.Asn164Lys
|
|
|
ENST00000568689.5:n.1880G>T
(JMJD8)
|
|
|
|
ENST00000569248.5:n.1123C>A
(STUB1)
|
|
|
|
ENST00000609261.5:c.*977G>T
(JMJD8)
|
ENSP00000477481.1:n.*977G>T
|
|
|
ENST00000620831.4:c.-50+38514C>A
(MSLN)
|
ENSP00000482893.1:n.-50+38514C>A
|
|
|
NM_001005920.2:c.*977G>T
(JMJD8)
|
NP_001005920.2:n.*977G>T
|
|
|
NM_001293197.1:c.333C>A
(STUB1)
|
NP_001280126.1:p.Asn111Lys
|
|
|
NM_005861.3:c.549C>A
(STUB1)
|
NP_005852.2:p.Asn183Lys
|
|
|
XM_005255295.3:c.*1011G>T
(JMJD8)
|
XP_005255352.1:n.*1011G>T
|
|
|
XM_005255297.3:c.*977G>T
(JMJD8)
|
XP_005255354.1:n.*977G>T
|
|
|
XM_011522474.1:c.*977G>T
(JMJD8)
|
XP_011520776.1:n.*977G>T
|
|
|
NM_001005920.3:c.*977G>T
(JMJD8)
|
NP_001005920.3:n.*977G>T
|
|
|
NM_001323918.2:c.*1011G>T
(JMJD8)
|
NP_001310847.2:n.*1011G>T
|
|
|
NM_001323919.2:c.*977G>T
(JMJD8)
|
NP_001310848.2:n.*977G>T
|
|
|
NM_001323920.2:c.*977G>T
(JMJD8)
|
NP_001310849.2:n.*977G>T
|
|
|
NM_001323922.2:c.*1011G>T
(JMJD8)
|
NP_001310851.2:n.*1011G>T
|
|
|
NR_136650.2:n.1870G>T
(JMJD8)
|
|
|
|
NR_136651.2:n.1875G>T
(JMJD8)
|
|
|
|
NR_136652.2:n.1785G>T
(JMJD8)
|
|
|
|
NM_001005920.4:c.*977G>T
(JMJD8)
MANE Select
|
NP_001005920.3:n.*977G>T
|
|
|
NM_005861.4:c.549C>A
(STUB1)
MANE Select
|
NP_005852.2:p.Asn183Lys
|
|
|
NM_001293197.2:c.333C>A
(STUB1)
|
NP_001280126.1:p.Asn111Lys
|
|
|
NM_001323918.3:c.*1011G>T
(JMJD8)
|
NP_001310847.2:n.*1011G>T
|
|
|
NM_001323919.3:c.*977G>T
(JMJD8)
|
NP_001310848.2:n.*977G>T
|
|
|
NM_001323920.3:c.*977G>T
(JMJD8)
|
NP_001310849.2:n.*977G>T
|
|
|
NM_001323922.3:c.*1011G>T
(JMJD8)
|
NP_001310851.2:n.*1011G>T
|
|
|
NR_136650.3:n.1870G>T
(JMJD8)
|
|
|
|
NR_136651.3:n.1875G>T
(JMJD8)
|
|
|
|
NR_136652.3:n.1785G>T
(JMJD8)
|
|
|
