ENST00000695651.1:n.2290A>C
|
|
|
ENST00000695653.1:c.1851A>C
|
ENSP00000512084.1:p.Glu617Asp
|
|
ENST00000695654.1:c.2967A>C
|
ENSP00000512085.1:p.Glu989Asp
|
|
ENST00000695690.1:n.133A>C
|
|
|
ENST00000695691.1:n.133A>C
|
|
|
ENST00000245907.11:c.3942A>C
MANE Select
|
ENSP00000245907.4:p.Glu1314Asp
|
|
ENST00000245907.10:c.3942A>C
|
ENSP00000245907.4:p.Glu1314Asp
|
|
ENST00000596238.1:n.385A>C
|
|
|
ENST00000596548.1:c.24A>C
|
ENSP00000469744.1:p.Glu8Asp
|
|
ENST00000601008.1:c.241+1731A>C
|
ENSP00000471384.1:n.241+1731A>C
|
|
NM_000064.3:c.3942A>C
|
NP_000055.2:p.Glu1314Asp
|
|
NM_000064.4:c.3942A>C
MANE Select
|
NP_000055.2:p.Glu1314Asp
|
|