ENST00000695651.1:n.2596T>C
|
|
|
ENST00000695653.1:c.2157T>C
|
ENSP00000512084.1:p.Asp719=
|
|
ENST00000695654.1:c.3273T>C
|
ENSP00000512085.1:p.Asp1091=
|
|
ENST00000695689.1:c.219T>C
|
ENSP00000512101.1:n.219T>C
|
|
ENST00000695690.1:n.439T>C
|
|
|
ENST00000695691.1:n.439T>C
|
|
|
ENST00000245907.11:c.4248T>C
MANE Select
|
ENSP00000245907.4:p.Asp1416=
|
|
ENST00000245907.10:c.4248T>C
|
ENSP00000245907.4:p.Asp1416=
|
|
ENST00000596548.1:c.369T>C
|
ENSP00000469744.1:p.Asp123=
|
|
ENST00000599899.5:n.1207T>C
|
|
|
ENST00000601008.1:c.242-4196T>C
|
ENSP00000471384.1:n.242-4196T>C
|
|
NM_000064.3:c.4248T>C
|
NP_000055.2:p.Asp1416=
|
|
NM_000064.4:c.4248T>C
MANE Select
|
NP_000055.2:p.Asp1416=
|
|