ENST00000369887.4:c.1319G>A
(CYP17A1)
MANE Select
|
ENSP00000358903.3:p.Arg440His
|
|
ENST00000638190.1:c.1016G>A
(CYP17A1)
|
ENSP00000492539.1:p.Arg339His
|
|
ENST00000638272.1:c.863G>A
(CYP17A1)
|
ENSP00000491508.1:p.Arg288His
|
|
ENST00000638971.1:c.1232G>A
(CYP17A1)
|
ENSP00000492313.1:p.Arg411His
|
|
ENST00000639393.1:c.1322G>A
(CYP17A1)
|
ENSP00000492651.1:p.Arg441His
|
|
ENST00000640633.1:n.1081G>A
(CYP17A1)
|
|
|
ENST00000647664.1:c.*592C>T
(WBP1L)
|
ENSP00000498131.1:n.*592C>T
|
|
ENST00000369887.3:c.1319G>A
(CYP17A1)
|
ENSP00000358903.3:p.Arg440His
|
|
NM_000102.3:c.1319G>A
(CYP17A1)
|
NP_000093.1:p.Arg440His
|
|
NM_000102.4:c.1319G>A
(CYP17A1)
MANE Select
|
NP_000093.1:p.Arg440His
|
|