ENST00000369887.4:c.1251C>T
(CYP17A1)
MANE Select
|
ENSP00000358903.3:p.Phe417=
|
|
ENST00000638190.1:c.948C>T
(CYP17A1)
|
ENSP00000492539.1:p.Phe316=
|
|
ENST00000638272.1:c.795C>T
(CYP17A1)
|
ENSP00000491508.1:p.Phe265=
|
|
ENST00000638971.1:c.1164C>T
(CYP17A1)
|
ENSP00000492313.1:p.Phe388=
|
|
ENST00000639393.1:c.1254C>T
(CYP17A1)
|
ENSP00000492651.1:p.Phe418=
|
|
ENST00000640633.1:n.1013C>T
(CYP17A1)
|
|
|
ENST00000647664.1:c.*628+32G>A
(WBP1L)
|
ENSP00000498131.1:n.*628+32G>A
|
|
ENST00000369887.3:c.1251C>T
(CYP17A1)
|
ENSP00000358903.3:p.Phe417=
|
|
ENST00000469683.1:n.204C>T
(CYP17A1)
|
|
|
NM_000102.3:c.1251C>T
(CYP17A1)
|
NP_000093.1:p.Phe417=
|
|
NM_000102.4:c.1251C>T
(CYP17A1)
MANE Select
|
NP_000093.1:p.Phe417=
|
|