ENST00000304874.14:c.837G=
MANE Select
|
ENSP00000307188.9:p.Thr279=
|
|
ENST00000362000.10:c.642G=
|
ENSP00000354710.6:p.Thr214=
|
|
ENST00000380839.9:c.759G=
|
ENSP00000370219.4:p.Thr253=
|
|
ENST00000395331.4:c.837G=
|
ENSP00000378740.3:p.Thr279=
|
|
ENST00000395332.8:c.837G=
|
ENSP00000378741.3:p.Thr279=
|
|
ENST00000488343.2:c.6G=
|
ENSP00000500864.1:p.Thr2=
|
|
ENST00000671817.1:c.759G=
|
ENSP00000500462.1:p.Thr253=
|
|
ENST00000672498.1:c.*136G=
|
ENSP00000500227.1:n.*136G=
|
|
ENST00000672586.1:n.1596G=
|
|
|
ENST00000672676.1:n.1861G=
|
|
|
ENST00000673149.1:n.649G=
|
|
|
ENST00000673350.1:n.2954G=
|
|
|
ENST00000673518.1:c.759G=
|
ENSP00000499889.1:p.Thr253=
|
|
ENST00000304874.13:c.837G=
|
ENSP00000307188.9:p.Thr279=
|
|
ENST00000362000.9:c.642G=
|
ENSP00000354710.5:p.Thr214=
|
|
ENST00000380839.8:c.759G=
|
ENSP00000370219.4:p.Thr253=
|
|
ENST00000395331.3:c.837G=
|
ENSP00000378740.3:p.Thr279=
|
|
ENST00000395332.7:c.837G=
|
ENSP00000378741.3:p.Thr279=
|
|
ENST00000450043.2:c.150G=
|
ENSP00000396527.2:p.Thr50=
|
|
ENST00000488343.1:n.6G=
|
|
|
ENST00000493708.5:n.218G=
|
|
|
NM_000048.3:c.837G=
|
NP_000039.2:p.Thr279=
|
|
NM_001024943.1:c.837G=
|
NP_001020114.1:p.Thr279=
|
|
NM_001024944.1:c.837G=
|
NP_001020115.1:p.Thr279=
|
|
NM_001024946.1:c.759G=
|
NP_001020117.1:p.Thr253=
|
|
NM_000048.4:c.837G=
MANE Select
|
NP_000039.2:p.Thr279=
|
|
NM_001024943.2:c.837G=
|
NP_001020114.1:p.Thr279=
|
|
NM_001024944.2:c.837G=
|
NP_001020115.1:p.Thr279=
|
|
NM_001024946.2:c.759G=
|
NP_001020117.1:p.Thr253=
|
|