ENST00000369887.4:c.1306G>T
(CYP17A1)
MANE Select
|
ENSP00000358903.3:p.Gly436Ter
|
|
ENST00000638190.1:c.1003G>T
(CYP17A1)
|
ENSP00000492539.1:p.Gly335Ter
|
|
ENST00000638272.1:c.850G>T
(CYP17A1)
|
ENSP00000491508.1:p.Gly284Ter
|
|
ENST00000638971.1:c.1219G>T
(CYP17A1)
|
ENSP00000492313.1:p.Gly407Ter
|
|
ENST00000639393.1:c.1309G>T
(CYP17A1)
|
ENSP00000492651.1:p.Gly437Ter
|
|
ENST00000640633.1:n.1068G>T
(CYP17A1)
|
|
|
ENST00000647664.1:c.*605C>A
(WBP1L)
|
ENSP00000498131.1:n.*605C>A
|
|
ENST00000369887.3:c.1306G>T
(CYP17A1)
|
ENSP00000358903.3:p.Gly436Ter
|
|
NM_000102.3:c.1306G>T
(CYP17A1)
|
NP_000093.1:p.Gly436Ter
|
|
NM_000102.4:c.1306G>T
(CYP17A1)
MANE Select
|
NP_000093.1:p.Gly436Ter
|
|