ENST00000369887.4:c.1301C>A
(CYP17A1)
MANE Select
|
ENSP00000358903.3:p.Pro434His
|
|
ENST00000638190.1:c.998C>A
(CYP17A1)
|
ENSP00000492539.1:p.Pro333His
|
|
ENST00000638272.1:c.845C>A
(CYP17A1)
|
ENSP00000491508.1:p.Pro282His
|
|
ENST00000638971.1:c.1214C>A
(CYP17A1)
|
ENSP00000492313.1:p.Pro405His
|
|
ENST00000639393.1:c.1304C>A
(CYP17A1)
|
ENSP00000492651.1:p.Pro435His
|
|
ENST00000640633.1:n.1063C>A
(CYP17A1)
|
|
|
ENST00000647664.1:c.*610G>T
(WBP1L)
|
ENSP00000498131.1:n.*610G>T
|
|
ENST00000369887.3:c.1301C>A
(CYP17A1)
|
ENSP00000358903.3:p.Pro434His
|
|
NM_000102.3:c.1301C>A
(CYP17A1)
|
NP_000093.1:p.Pro434His
|
|
NM_000102.4:c.1301C>A
(CYP17A1)
MANE Select
|
NP_000093.1:p.Pro434His
|
|