ENST00000695651.1:n.924A>G
|
|
|
ENST00000695652.1:c.2453A>G
|
ENSP00000512083.1:p.Glu818Gly
|
|
ENST00000695653.1:c.485A>G
|
ENSP00000512084.1:p.Glu162Gly
|
|
ENST00000695654.1:c.1700A>G
|
ENSP00000512085.1:p.Glu567Gly
|
|
ENST00000695655.1:c.1517A>G
|
ENSP00000512086.1:n.1517A>G
|
|
ENST00000695692.1:n.1940A>G
|
|
|
ENST00000245907.11:c.2576A>G
MANE Select
|
ENSP00000245907.4:p.Glu859Gly
|
|
ENST00000245907.10:c.2576A>G
|
ENSP00000245907.4:p.Glu859Gly
|
|
ENST00000594005.1:n.57A>G
|
|
|
NM_000064.3:c.2576A>G
|
NP_000055.2:p.Glu859Gly
|
|
NM_000064.4:c.2576A>G
MANE Select
|
NP_000055.2:p.Glu859Gly
|
|