ENST00000369887.4:c.1433G>T
(CYP17A1)
MANE Select
|
ENSP00000358903.3:p.Gly478Val
|
|
ENST00000638190.1:c.1130G>T
(CYP17A1)
|
ENSP00000492539.1:p.Gly377Val
|
|
ENST00000638272.1:c.977G>T
(CYP17A1)
|
ENSP00000491508.1:p.Gly326Val
|
|
ENST00000638971.1:c.1346G>T
(CYP17A1)
|
ENSP00000492313.1:p.Gly449Val
|
|
ENST00000639393.1:c.1436G>T
(CYP17A1)
|
ENSP00000492651.1:p.Gly479Val
|
|
ENST00000640633.1:n.1195G>T
(CYP17A1)
|
|
|
ENST00000647664.1:c.*478C>A
(WBP1L)
|
ENSP00000498131.1:n.*478C>A
|
|
ENST00000369887.3:c.1433G>T
(CYP17A1)
|
ENSP00000358903.3:p.Gly478Val
|
|
NM_000102.3:c.1433G>T
(CYP17A1)
|
NP_000093.1:p.Gly478Val
|
|
NM_000102.4:c.1433G>T
(CYP17A1)
MANE Select
|
NP_000093.1:p.Gly478Val
|
|