ENST00000369887.4:c.1345C>G
(CYP17A1)
MANE Select
|
ENSP00000358903.3:p.Arg449Gly
|
|
ENST00000638190.1:c.1042C>G
(CYP17A1)
|
ENSP00000492539.1:p.Arg348Gly
|
|
ENST00000638272.1:c.889C>G
(CYP17A1)
|
ENSP00000491508.1:p.Arg297Gly
|
|
ENST00000638971.1:c.1258C>G
(CYP17A1)
|
ENSP00000492313.1:p.Arg420Gly
|
|
ENST00000639393.1:c.1348C>G
(CYP17A1)
|
ENSP00000492651.1:p.Arg450Gly
|
|
ENST00000640633.1:n.1107C>G
(CYP17A1)
|
|
|
ENST00000647664.1:c.*566G>C
(WBP1L)
|
ENSP00000498131.1:n.*566G>C
|
|
ENST00000369887.3:c.1345C>G
(CYP17A1)
|
ENSP00000358903.3:p.Arg449Gly
|
|
NM_000102.3:c.1345C>G
(CYP17A1)
|
NP_000093.1:p.Arg449Gly
|
|
NM_000102.4:c.1345C>G
(CYP17A1)
MANE Select
|
NP_000093.1:p.Arg449Gly
|
|