ENST00000470094.2:c.*387A>G
|
ENSP00000434898.2:n.*387A>G
|
|
ENST00000528762.2:c.*1231A>G
|
ENSP00000433168.2:n.*1231A>G
|
|
ENST00000530893.7:c.9495A>G
|
ENSP00000499438.2:p.Thr3165=
|
|
ENST00000665585.2:c.*1426A>G
|
ENSP00000499570.2:n.*1426A>G
|
|
ENST00000700202.2:c.9813A>G
|
ENSP00000514856.2:p.Thr3271=
|
|
ENST00000700202.1:c.2280A>G
|
ENSP00000514856.1:p.Thr760=
|
|
ENST00000700203.1:n.1991A>G
|
|
|
ENST00000380152.8:c.9864A>G
MANE Select
|
ENSP00000369497.3:p.Thr3288=
|
|
ENST00000544455.6:c.9864A>G
|
ENSP00000439902.1:p.Thr3288=
|
|
ENST00000614259.2:c.9872A>G
|
ENSP00000506251.1:n.9872A>G
|
|
ENST00000680887.1:c.9864A>G
|
ENSP00000505508.1:p.Thr3288=
|
|
ENST00000380152.7:c.9864A>G
|
ENSP00000369497.3:p.Thr3288=
|
|
ENST00000533776.1:n.452A>G
|
|
|
ENST00000544455.5:c.9864A>G
|
ENSP00000439902.1:p.Thr3288=
|
|
NM_000059.3:c.9864A>G , LRG_293t1:c.9864A>G
|
NP_000050.2:p.Thr3288=
|
|
XM_011535203.1:c.9864A>G
|
XP_011533505.1:p.Thr3288=
|
|
XM_011535204.1:c.9768A>G
|
XP_011533506.1:p.Thr3256=
|
|
NM_000059.4:c.9864A>G
MANE Select
|
NP_000050.3:p.Thr3288=
|
|