ENST00000695651.1:n.2870G>C
|
|
|
ENST00000695653.1:c.2431G>C
|
ENSP00000512084.1:p.Asp811His
|
|
ENST00000695654.1:c.3547G>C
|
ENSP00000512085.1:p.Asp1183His
|
|
ENST00000695689.1:c.493G>C
|
ENSP00000512101.1:n.493G>C
|
|
ENST00000695690.1:n.1587G>C
|
|
|
ENST00000695691.1:n.1383G>C
|
|
|
ENST00000245907.11:c.4522G>C
MANE Select
|
ENSP00000245907.4:p.Asp1508His
|
|
ENST00000245907.10:c.4522G>C
|
ENSP00000245907.4:p.Asp1508His
|
|
ENST00000599668.1:n.117G>C
|
|
|
ENST00000599899.5:n.1481G>C
|
|
|
ENST00000601008.1:c.242-1473G>C
|
ENSP00000471384.1:n.242-1473G>C
|
|
NM_000064.3:c.4522G>C
|
NP_000055.2:p.Asp1508His
|
|
NM_000064.4:c.4522G>C
MANE Select
|
NP_000055.2:p.Asp1508His
|
|