ENST00000695651.1:n.1119G>T
|
|
|
ENST00000695652.1:c.2648G>T
|
ENSP00000512083.1:p.Gly883Val
|
|
ENST00000695653.1:c.680G>T
|
ENSP00000512084.1:p.Gly227Val
|
|
ENST00000695654.1:c.1895G>T
|
ENSP00000512085.1:p.Gly632Val
|
|
ENST00000695655.1:c.1712G>T
|
ENSP00000512086.1:n.1712G>T
|
|
ENST00000695692.1:n.2135G>T
|
|
|
ENST00000245907.11:c.2771G>T
MANE Select
|
ENSP00000245907.4:p.Gly924Val
|
|
ENST00000245907.10:c.2771G>T
|
ENSP00000245907.4:p.Gly924Val
|
|
ENST00000594005.1:n.347G>T
|
|
|
NM_000064.3:c.2771G>T
|
NP_000055.2:p.Gly924Val
|
|
NM_000064.4:c.2771G>T
MANE Select
|
NP_000055.2:p.Gly924Val
|
|