ENST00000369887.4:c.1240C>G
(CYP17A1)
MANE Select
|
ENSP00000358903.3:p.Pro414Ala
|
|
ENST00000638190.1:c.937C>G
(CYP17A1)
|
ENSP00000492539.1:p.Pro313Ala
|
|
ENST00000638272.1:c.784C>G
(CYP17A1)
|
ENSP00000491508.1:p.Pro262Ala
|
|
ENST00000638971.1:c.1153C>G
(CYP17A1)
|
ENSP00000492313.1:p.Pro385Ala
|
|
ENST00000639393.1:c.1243C>G
(CYP17A1)
|
ENSP00000492651.1:p.Pro415Ala
|
|
ENST00000640633.1:n.1002C>G
(CYP17A1)
|
|
|
ENST00000647664.1:c.*629-87G>C
(WBP1L)
|
ENSP00000498131.1:n.*629-87G>C
|
|
ENST00000369887.3:c.1240C>G
(CYP17A1)
|
ENSP00000358903.3:p.Pro414Ala
|
|
ENST00000469683.1:n.193C>G
(CYP17A1)
|
|
|
NM_000102.3:c.1240C>G
(CYP17A1)
|
NP_000093.1:p.Pro414Ala
|
|
NM_000102.4:c.1240C>G
(CYP17A1)
MANE Select
|
NP_000093.1:p.Pro414Ala
|
|