ENST00000369887.4:c.1276A>G
(CYP17A1)
MANE Select
|
ENSP00000358903.3:p.Ile426Val
|
|
ENST00000638190.1:c.973A>G
(CYP17A1)
|
ENSP00000492539.1:p.Ile325Val
|
|
ENST00000638272.1:c.820A>G
(CYP17A1)
|
ENSP00000491508.1:p.Ile274Val
|
|
ENST00000638971.1:c.1189A>G
(CYP17A1)
|
ENSP00000492313.1:p.Ile397Val
|
|
ENST00000639393.1:c.1279A>G
(CYP17A1)
|
ENSP00000492651.1:p.Ile427Val
|
|
ENST00000640633.1:n.1038A>G
(CYP17A1)
|
|
|
ENST00000647664.1:c.*628+7T>C
(WBP1L)
|
ENSP00000498131.1:n.*628+7T>C
|
|
ENST00000369887.3:c.1276A>G
(CYP17A1)
|
ENSP00000358903.3:p.Ile426Val
|
|
ENST00000469683.1:n.229A>G
(CYP17A1)
|
|
|
NM_000102.3:c.1276A>G
(CYP17A1)
|
NP_000093.1:p.Ile426Val
|
|
NM_000102.4:c.1276A>G
(CYP17A1)
MANE Select
|
NP_000093.1:p.Ile426Val
|
|