ENST00000369887.4:c.1238T>C
(CYP17A1)
MANE Select
|
ENSP00000358903.3:p.Met413Thr
|
|
ENST00000638190.1:c.935T>C
(CYP17A1)
|
ENSP00000492539.1:p.Met312Thr
|
|
ENST00000638272.1:c.782T>C
(CYP17A1)
|
ENSP00000491508.1:p.Met261Thr
|
|
ENST00000638971.1:c.1151T>C
(CYP17A1)
|
ENSP00000492313.1:p.Met384Thr
|
|
ENST00000639393.1:c.1241T>C
(CYP17A1)
|
ENSP00000492651.1:p.Met414Thr
|
|
ENST00000640633.1:n.1000T>C
(CYP17A1)
|
|
|
ENST00000647664.1:c.*629-85A>G
(WBP1L)
|
ENSP00000498131.1:n.*629-85A>G
|
|
ENST00000369887.3:c.1238T>C
(CYP17A1)
|
ENSP00000358903.3:p.Met413Thr
|
|
ENST00000469683.1:n.191T>C
(CYP17A1)
|
|
|
NM_000102.3:c.1238T>C
(CYP17A1)
|
NP_000093.1:p.Met413Thr
|
|
NM_000102.4:c.1238T>C
(CYP17A1)
MANE Select
|
NP_000093.1:p.Met413Thr
|
|