ENST00000253122.10:c.1389T>A
MANE Select
|
ENSP00000253122.5:p.Thr463=
|
|
ENST00000253122.9:c.1389T>A
|
ENSP00000253122.5:p.Thr463=
|
|
ENST00000413787.1:c.318T>A
|
ENSP00000400463.1:p.Thr106=
|
|
ENST00000430077.6:c.1044T>A
|
ENSP00000403041.2:p.Thr348=
|
|
ENST00000442457.1:c.443T>A
|
|
|
ENST00000485324.1:n.1534T>A
|
|
|
NM_001142805.1:c.1359T>A
|
NP_001136277.1:p.Thr453=
|
|
NM_001142806.1:c.1044T>A
|
NP_001136278.1:p.Thr348=
|
|
NM_005629.3:c.1389T>A
|
NP_005620.1:p.Thr463=
|
|
NM_005629.4:c.1389T>A
MANE Select
|
NP_005620.1:p.Thr463=
|
|
NM_001142805.2:c.1359T>A
|
NP_001136277.1:p.Thr453=
|
|