ENST00000369887.4:c.1342G>A
(CYP17A1)
MANE Select
|
ENSP00000358903.3:p.Ala448Thr
|
|
ENST00000638190.1:c.1039G>A
(CYP17A1)
|
ENSP00000492539.1:p.Ala347Thr
|
|
ENST00000638272.1:c.886G>A
(CYP17A1)
|
ENSP00000491508.1:p.Ala296Thr
|
|
ENST00000638971.1:c.1255G>A
(CYP17A1)
|
ENSP00000492313.1:p.Ala419Thr
|
|
ENST00000639393.1:c.1345G>A
(CYP17A1)
|
ENSP00000492651.1:p.Ala449Thr
|
|
ENST00000640633.1:n.1104G>A
(CYP17A1)
|
|
|
ENST00000647664.1:c.*569C>T
(WBP1L)
|
ENSP00000498131.1:n.*569C>T
|
|
ENST00000369887.3:c.1342G>A
(CYP17A1)
|
ENSP00000358903.3:p.Ala448Thr
|
|
NM_000102.3:c.1342G>A
(CYP17A1)
|
NP_000093.1:p.Ala448Thr
|
|
NM_000102.4:c.1342G>A
(CYP17A1)
MANE Select
|
NP_000093.1:p.Ala448Thr
|
|