ENST00000695651.1:n.2087G>T
|
|
|
ENST00000695652.1:c.3616G>T
|
ENSP00000512083.1:p.Asp1206Tyr
|
|
ENST00000695653.1:c.1648G>T
|
ENSP00000512084.1:p.Asp550Tyr
|
|
ENST00000695654.1:c.2764G>T
|
ENSP00000512085.1:p.Asp922Tyr
|
|
ENST00000695655.1:c.2680G>T
|
ENSP00000512086.1:n.2680G>T
|
|
ENST00000695692.1:n.3103G>T
|
|
|
ENST00000245907.11:c.3739G>T
MANE Select
|
ENSP00000245907.4:p.Asp1247Tyr
|
|
ENST00000245907.10:c.3739G>T
|
ENSP00000245907.4:p.Asp1247Tyr
|
|
ENST00000596238.1:n.182G>T
|
|
|
ENST00000601008.1:c.241+551G>T
|
ENSP00000471384.1:n.241+551G>T
|
|
NM_000064.3:c.3739G>T
|
NP_000055.2:p.Asp1247Tyr
|
|
NM_000064.4:c.3739G>T
MANE Select
|
NP_000055.2:p.Asp1247Tyr
|
|