ENST00000369887.4:c.1332T>G
(CYP17A1)
MANE Select
|
ENSP00000358903.3:p.Gly444=
|
|
ENST00000638190.1:c.1029T>G
(CYP17A1)
|
ENSP00000492539.1:p.Gly343=
|
|
ENST00000638272.1:c.876T>G
(CYP17A1)
|
ENSP00000491508.1:p.Gly292=
|
|
ENST00000638971.1:c.1245T>G
(CYP17A1)
|
ENSP00000492313.1:p.Gly415=
|
|
ENST00000639393.1:c.1335T>G
(CYP17A1)
|
ENSP00000492651.1:p.Gly445=
|
|
ENST00000640633.1:n.1094T>G
(CYP17A1)
|
|
|
ENST00000647664.1:c.*579A>C
(WBP1L)
|
ENSP00000498131.1:n.*579A>C
|
|
ENST00000369887.3:c.1332T>G
(CYP17A1)
|
ENSP00000358903.3:p.Gly444=
|
|
NM_000102.3:c.1332T>G
(CYP17A1)
|
NP_000093.1:p.Gly444=
|
|
NM_000102.4:c.1332T>G
(CYP17A1)
MANE Select
|
NP_000093.1:p.Gly444=
|
|