ENST00000369887.4:c.1261G>T
(CYP17A1)
MANE Select
|
ENSP00000358903.3:p.Ala421Ser
|
|
ENST00000638190.1:c.958G>T
(CYP17A1)
|
ENSP00000492539.1:p.Ala320Ser
|
|
ENST00000638272.1:c.805G>T
(CYP17A1)
|
ENSP00000491508.1:p.Ala269Ser
|
|
ENST00000638971.1:c.1174G>T
(CYP17A1)
|
ENSP00000492313.1:p.Ala392Ser
|
|
ENST00000639393.1:c.1264G>T
(CYP17A1)
|
ENSP00000492651.1:p.Ala422Ser
|
|
ENST00000640633.1:n.1023G>T
(CYP17A1)
|
|
|
ENST00000647664.1:c.*628+22C>A
(WBP1L)
|
ENSP00000498131.1:n.*628+22C>A
|
|
ENST00000369887.3:c.1261G>T
(CYP17A1)
|
ENSP00000358903.3:p.Ala421Ser
|
|
ENST00000469683.1:n.214G>T
(CYP17A1)
|
|
|
NM_000102.3:c.1261G>T
(CYP17A1)
|
NP_000093.1:p.Ala421Ser
|
|
NM_000102.4:c.1261G>T
(CYP17A1)
MANE Select
|
NP_000093.1:p.Ala421Ser
|
|