ENST00000369887.4:c.1331G>T
(CYP17A1)
MANE Select
|
ENSP00000358903.3:p.Gly444Val
|
|
ENST00000638190.1:c.1028G>T
(CYP17A1)
|
ENSP00000492539.1:p.Gly343Val
|
|
ENST00000638272.1:c.875G>T
(CYP17A1)
|
ENSP00000491508.1:p.Gly292Val
|
|
ENST00000638971.1:c.1244G>T
(CYP17A1)
|
ENSP00000492313.1:p.Gly415Val
|
|
ENST00000639393.1:c.1334G>T
(CYP17A1)
|
ENSP00000492651.1:p.Gly445Val
|
|
ENST00000640633.1:n.1093G>T
(CYP17A1)
|
|
|
ENST00000647664.1:c.*580C>A
(WBP1L)
|
ENSP00000498131.1:n.*580C>A
|
|
ENST00000369887.3:c.1331G>T
(CYP17A1)
|
ENSP00000358903.3:p.Gly444Val
|
|
NM_000102.3:c.1331G>T
(CYP17A1)
|
NP_000093.1:p.Gly444Val
|
|
NM_000102.4:c.1331G>T
(CYP17A1)
MANE Select
|
NP_000093.1:p.Gly444Val
|
|