ENST00000369887.4:c.1272G>C
(CYP17A1)
MANE Select
|
ENSP00000358903.3:p.Gln424His
|
|
ENST00000638190.1:c.969G>C
(CYP17A1)
|
ENSP00000492539.1:p.Gln323His
|
|
ENST00000638272.1:c.816G>C
(CYP17A1)
|
ENSP00000491508.1:p.Gln272His
|
|
ENST00000638971.1:c.1185G>C
(CYP17A1)
|
ENSP00000492313.1:p.Gln395His
|
|
ENST00000639393.1:c.1275G>C
(CYP17A1)
|
ENSP00000492651.1:p.Gln425His
|
|
ENST00000640633.1:n.1034G>C
(CYP17A1)
|
|
|
ENST00000647664.1:c.*628+11C>G
(WBP1L)
|
ENSP00000498131.1:n.*628+11C>G
|
|
ENST00000369887.3:c.1272G>C
(CYP17A1)
|
ENSP00000358903.3:p.Gln424His
|
|
ENST00000469683.1:n.225G>C
(CYP17A1)
|
|
|
NM_000102.3:c.1272G>C
(CYP17A1)
|
NP_000093.1:p.Gln424His
|
|
NM_000102.4:c.1272G>C
(CYP17A1)
MANE Select
|
NP_000093.1:p.Gln424His
|
|