ENST00000369887.4:c.1303T>G
(CYP17A1)
MANE Select
|
ENSP00000358903.3:p.Phe435Val
|
|
ENST00000638190.1:c.1000T>G
(CYP17A1)
|
ENSP00000492539.1:p.Phe334Val
|
|
ENST00000638272.1:c.847T>G
(CYP17A1)
|
ENSP00000491508.1:p.Phe283Val
|
|
ENST00000638971.1:c.1216T>G
(CYP17A1)
|
ENSP00000492313.1:p.Phe406Val
|
|
ENST00000639393.1:c.1306T>G
(CYP17A1)
|
ENSP00000492651.1:p.Phe436Val
|
|
ENST00000640633.1:n.1065T>G
(CYP17A1)
|
|
|
ENST00000647664.1:c.*608A>C
(WBP1L)
|
ENSP00000498131.1:n.*608A>C
|
|
ENST00000369887.3:c.1303T>G
(CYP17A1)
|
ENSP00000358903.3:p.Phe435Val
|
|
NM_000102.3:c.1303T>G
(CYP17A1)
|
NP_000093.1:p.Phe435Val
|
|
NM_000102.4:c.1303T>G
(CYP17A1)
MANE Select
|
NP_000093.1:p.Phe435Val
|
|