ENST00000695651.1:n.2073A>G
|
|
|
ENST00000695652.1:c.3602A>G
|
ENSP00000512083.1:p.Gln1201Arg
|
|
ENST00000695653.1:c.1634A>G
|
ENSP00000512084.1:p.Gln545Arg
|
|
ENST00000695654.1:c.2750A>G
|
ENSP00000512085.1:p.Gln917Arg
|
|
ENST00000695655.1:c.2666A>G
|
ENSP00000512086.1:n.2666A>G
|
|
ENST00000695692.1:n.3089A>G
|
|
|
ENST00000245907.11:c.3725A>G
MANE Select
|
ENSP00000245907.4:p.Gln1242Arg
|
|
ENST00000245907.10:c.3725A>G
|
ENSP00000245907.4:p.Gln1242Arg
|
|
ENST00000596238.1:n.168A>G
|
|
|
ENST00000601008.1:c.241+537A>G
|
ENSP00000471384.1:n.241+537A>G
|
|
NM_000064.3:c.3725A>G
|
NP_000055.2:p.Gln1242Arg
|
|
NM_000064.4:c.3725A>G
MANE Select
|
NP_000055.2:p.Gln1242Arg
|
|