ENST00000470094.2:c.*453A>G
|
ENSP00000434898.2:n.*453A>G
|
|
ENST00000528762.2:c.*1297A>G
|
ENSP00000433168.2:n.*1297A>G
|
|
ENST00000530893.7:c.9561A>G
|
ENSP00000499438.2:p.Thr3187=
|
|
ENST00000665585.2:c.*1492A>G
|
ENSP00000499570.2:n.*1492A>G
|
|
ENST00000700202.2:c.9879A>G
|
ENSP00000514856.2:p.Thr3293=
|
|
ENST00000700202.1:c.2346A>G
|
ENSP00000514856.1:p.Thr782=
|
|
ENST00000700203.1:n.2057A>G
|
|
|
ENST00000380152.8:c.9930A>G
MANE Select
|
ENSP00000369497.3:p.Thr3310=
|
|
ENST00000544455.6:c.9930A>G
|
ENSP00000439902.1:p.Thr3310=
|
|
ENST00000614259.2:c.9938A>G
|
ENSP00000506251.1:n.9938A>G
|
|
ENST00000680887.1:c.9930A>G
|
ENSP00000505508.1:p.Thr3310=
|
|
ENST00000380152.7:c.9930A>G
|
ENSP00000369497.3:p.Thr3310=
|
|
ENST00000533776.1:n.518A>G
|
|
|
ENST00000544455.5:c.9930A>G
|
ENSP00000439902.1:p.Thr3310=
|
|
NM_000059.3:c.9930A>G , LRG_293t1:c.9930A>G
|
NP_000050.2:p.Thr3310=
|
|
XM_011535203.1:c.9930A>G
|
XP_011533505.1:p.Thr3310=
|
|
XM_011535204.1:c.9834A>G
|
XP_011533506.1:p.Thr3278=
|
|
NM_000059.4:c.9930A>G
MANE Select
|
NP_000050.3:p.Thr3310=
|
|