ENST00000369887.4:c.1325G>A
(CYP17A1)
MANE Select
|
ENSP00000358903.3:p.Cys442Tyr
|
|
ENST00000638190.1:c.1022G>A
(CYP17A1)
|
ENSP00000492539.1:p.Cys341Tyr
|
|
ENST00000638272.1:c.869G>A
(CYP17A1)
|
ENSP00000491508.1:p.Cys290Tyr
|
|
ENST00000638971.1:c.1238G>A
(CYP17A1)
|
ENSP00000492313.1:p.Cys413Tyr
|
|
ENST00000639393.1:c.1328G>A
(CYP17A1)
|
ENSP00000492651.1:p.Cys443Tyr
|
|
ENST00000640633.1:n.1087G>A
(CYP17A1)
|
|
|
ENST00000647664.1:c.*586C>T
(WBP1L)
|
ENSP00000498131.1:n.*586C>T
|
|
ENST00000369887.3:c.1325G>A
(CYP17A1)
|
ENSP00000358903.3:p.Cys442Tyr
|
|
NM_000102.3:c.1325G>A
(CYP17A1)
|
NP_000093.1:p.Cys442Tyr
|
|
NM_000102.4:c.1325G>A
(CYP17A1)
MANE Select
|
NP_000093.1:p.Cys442Tyr
|
|