ENST00000695651.1:n.2103T>G
|
|
|
ENST00000695652.1:c.3632T>G
|
ENSP00000512083.1:p.Val1211Gly
|
|
ENST00000695653.1:c.1664T>G
|
ENSP00000512084.1:p.Val555Gly
|
|
ENST00000695654.1:c.2780T>G
|
ENSP00000512085.1:p.Val927Gly
|
|
ENST00000695655.1:c.2696T>G
|
ENSP00000512086.1:n.2696T>G
|
|
ENST00000695692.1:n.3119T>G
|
|
|
ENST00000245907.11:c.3755T>G
MANE Select
|
ENSP00000245907.4:p.Val1252Gly
|
|
ENST00000245907.10:c.3755T>G
|
ENSP00000245907.4:p.Val1252Gly
|
|
ENST00000596238.1:n.198T>G
|
|
|
ENST00000601008.1:c.241+567T>G
|
ENSP00000471384.1:n.241+567T>G
|
|
NM_000064.3:c.3755T>G
|
NP_000055.2:p.Val1252Gly
|
|
NM_000064.4:c.3755T>G
MANE Select
|
NP_000055.2:p.Val1252Gly
|
|