ENST00000369887.4:c.1252T>G
(CYP17A1)
MANE Select
|
ENSP00000358903.3:p.Leu418Val
|
|
ENST00000638190.1:c.949T>G
(CYP17A1)
|
ENSP00000492539.1:p.Leu317Val
|
|
ENST00000638272.1:c.796T>G
(CYP17A1)
|
ENSP00000491508.1:p.Leu266Val
|
|
ENST00000638971.1:c.1165T>G
(CYP17A1)
|
ENSP00000492313.1:p.Leu389Val
|
|
ENST00000639393.1:c.1255T>G
(CYP17A1)
|
ENSP00000492651.1:p.Leu419Val
|
|
ENST00000640633.1:n.1014T>G
(CYP17A1)
|
|
|
ENST00000647664.1:c.*628+31A>C
(WBP1L)
|
ENSP00000498131.1:n.*628+31A>C
|
|
ENST00000369887.3:c.1252T>G
(CYP17A1)
|
ENSP00000358903.3:p.Leu418Val
|
|
ENST00000469683.1:n.205T>G
(CYP17A1)
|
|
|
NM_000102.3:c.1252T>G
(CYP17A1)
|
NP_000093.1:p.Leu418Val
|
|
NM_000102.4:c.1252T>G
(CYP17A1)
MANE Select
|
NP_000093.1:p.Leu418Val
|
|