ENST00000369887.4:c.1313G>C
(CYP17A1)
MANE Select
|
ENSP00000358903.3:p.Gly438Ala
|
|
ENST00000638190.1:c.1010G>C
(CYP17A1)
|
ENSP00000492539.1:p.Gly337Ala
|
|
ENST00000638272.1:c.857G>C
(CYP17A1)
|
ENSP00000491508.1:p.Gly286Ala
|
|
ENST00000638971.1:c.1226G>C
(CYP17A1)
|
ENSP00000492313.1:p.Gly409Ala
|
|
ENST00000639393.1:c.1316G>C
(CYP17A1)
|
ENSP00000492651.1:p.Gly439Ala
|
|
ENST00000640633.1:n.1075G>C
(CYP17A1)
|
|
|
ENST00000647664.1:c.*598C>G
(WBP1L)
|
ENSP00000498131.1:n.*598C>G
|
|
ENST00000369887.3:c.1313G>C
(CYP17A1)
|
ENSP00000358903.3:p.Gly438Ala
|
|
NM_000102.3:c.1313G>C
(CYP17A1)
|
NP_000093.1:p.Gly438Ala
|
|
NM_000102.4:c.1313G>C
(CYP17A1)
MANE Select
|
NP_000093.1:p.Gly438Ala
|
|