ENST00000695651.1:n.867T>G
|
|
|
ENST00000695652.1:c.2396T>G
|
ENSP00000512083.1:p.Val799Gly
|
|
ENST00000695653.1:c.428T>G
|
ENSP00000512084.1:p.Val143Gly
|
|
ENST00000695654.1:c.1643T>G
|
ENSP00000512085.1:p.Val548Gly
|
|
ENST00000695655.1:c.1460T>G
|
ENSP00000512086.1:n.1460T>G
|
|
ENST00000695692.1:n.1883T>G
|
|
|
ENST00000245907.11:c.2519T>G
MANE Select
|
ENSP00000245907.4:p.Val840Gly
|
|
ENST00000245907.10:c.2519T>G
|
ENSP00000245907.4:p.Val840Gly
|
|
ENST00000602053.1:n.567T>G
|
|
|
NM_000064.3:c.2519T>G
|
NP_000055.2:p.Val840Gly
|
|
NM_000064.4:c.2519T>G
MANE Select
|
NP_000055.2:p.Val840Gly
|
|