ENST00000369884.4:n.152-132T>A
|
|
|
ENST00000369887.4:c.744A>T
(CYP17A1)
MANE Select
|
ENSP00000358903.3:p.Glu248Asp
|
|
ENST00000638190.1:c.666+740A>T
(CYP17A1)
|
ENSP00000492539.1:n.666+740A>T
|
|
ENST00000638272.1:c.298-837A>T
(CYP17A1)
|
ENSP00000491508.1:n.298-837A>T
|
|
ENST00000638971.1:c.666+740A>T
(CYP17A1)
|
ENSP00000492313.1:n.666+740A>T
|
|
ENST00000639393.1:c.744A>T
(CYP17A1)
|
ENSP00000492651.1:p.Glu248Asp
|
|
ENST00000640633.1:n.506A>T
(CYP17A1)
|
|
|
ENST00000369887.3:c.744A>T
(CYP17A1)
|
ENSP00000358903.3:p.Glu248Asp
|
|
ENST00000489268.1:n.1660A>T
(CYP17A1)
|
|
|
NM_000102.3:c.744A>T
(CYP17A1)
|
NP_000093.1:p.Glu248Asp
|
|
XR_428804.1:n.206-132T>A
(CYP17A1-AS1)
|
|
|
NM_000102.4:c.744A>T
(CYP17A1)
MANE Select
|
NP_000093.1:p.Glu248Asp
|
|