ENST00000369887.4:c.1274T>G
(CYP17A1)
MANE Select
|
ENSP00000358903.3:p.Leu425Arg
|
|
ENST00000638190.1:c.971T>G
(CYP17A1)
|
ENSP00000492539.1:p.Leu324Arg
|
|
ENST00000638272.1:c.818T>G
(CYP17A1)
|
ENSP00000491508.1:p.Leu273Arg
|
|
ENST00000638971.1:c.1187T>G
(CYP17A1)
|
ENSP00000492313.1:p.Leu396Arg
|
|
ENST00000639393.1:c.1277T>G
(CYP17A1)
|
ENSP00000492651.1:p.Leu426Arg
|
|
ENST00000640633.1:n.1036T>G
(CYP17A1)
|
|
|
ENST00000647664.1:c.*628+9A>C
(WBP1L)
|
ENSP00000498131.1:n.*628+9A>C
|
|
ENST00000369887.3:c.1274T>G
(CYP17A1)
|
ENSP00000358903.3:p.Leu425Arg
|
|
ENST00000469683.1:n.227T>G
(CYP17A1)
|
|
|
NM_000102.3:c.1274T>G
(CYP17A1)
|
NP_000093.1:p.Leu425Arg
|
|
NM_000102.4:c.1274T>G
(CYP17A1)
MANE Select
|
NP_000093.1:p.Leu425Arg
|
|