ENST00000369887.4:c.1228G>T
(CYP17A1)
MANE Select
|
ENSP00000358903.3:p.Asp410Tyr
|
|
ENST00000638190.1:c.925G>T
(CYP17A1)
|
ENSP00000492539.1:p.Asp309Tyr
|
|
ENST00000638272.1:c.772G>T
(CYP17A1)
|
ENSP00000491508.1:p.Asp258Tyr
|
|
ENST00000638971.1:c.1141G>T
(CYP17A1)
|
ENSP00000492313.1:p.Asp381Tyr
|
|
ENST00000639393.1:c.1231G>T
(CYP17A1)
|
ENSP00000492651.1:p.Asp411Tyr
|
|
ENST00000640633.1:n.990G>T
(CYP17A1)
|
|
|
ENST00000647664.1:c.*629-75C>A
(WBP1L)
|
ENSP00000498131.1:n.*629-75C>A
|
|
ENST00000369887.3:c.1228G>T
(CYP17A1)
|
ENSP00000358903.3:p.Asp410Tyr
|
|
ENST00000469683.1:n.181G>T
(CYP17A1)
|
|
|
NM_000102.3:c.1228G>T
(CYP17A1)
|
NP_000093.1:p.Asp410Tyr
|
|
NM_000102.4:c.1228G>T
(CYP17A1)
MANE Select
|
NP_000093.1:p.Asp410Tyr
|
|