ENST00000695651.1:n.1143T>G
|
|
|
ENST00000695652.1:c.2672T>G
|
ENSP00000512083.1:p.Val891Gly
|
|
ENST00000695653.1:c.704T>G
|
ENSP00000512084.1:p.Val235Gly
|
|
ENST00000695654.1:c.1919T>G
|
ENSP00000512085.1:p.Val640Gly
|
|
ENST00000695655.1:c.1736T>G
|
ENSP00000512086.1:n.1736T>G
|
|
ENST00000695692.1:n.2159T>G
|
|
|
ENST00000245907.11:c.2795T>G
MANE Select
|
ENSP00000245907.4:p.Val932Gly
|
|
ENST00000245907.10:c.2795T>G
|
ENSP00000245907.4:p.Val932Gly
|
|
ENST00000594005.1:n.371T>G
|
|
|
NM_000064.3:c.2795T>G
|
NP_000055.2:p.Val932Gly
|
|
NM_000064.4:c.2795T>G
MANE Select
|
NP_000055.2:p.Val932Gly
|
|