ENST00000470094.2:c.*386C>G
|
ENSP00000434898.2:n.*386C>G
|
|
ENST00000528762.2:c.*1230C>G
|
ENSP00000433168.2:n.*1230C>G
|
|
ENST00000530893.7:c.9494C>G
|
ENSP00000499438.2:p.Thr3165Arg
|
|
ENST00000665585.2:c.*1425C>G
|
ENSP00000499570.2:n.*1425C>G
|
|
ENST00000700202.2:c.9812C>G
|
ENSP00000514856.2:p.Thr3271Arg
|
|
ENST00000700202.1:c.2279C>G
|
ENSP00000514856.1:p.Thr760Arg
|
|
ENST00000700203.1:n.1990C>G
|
|
|
ENST00000380152.8:c.9863C>G
MANE Select
|
ENSP00000369497.3:p.Thr3288Arg
|
|
ENST00000544455.6:c.9863C>G
|
ENSP00000439902.1:p.Thr3288Arg
|
|
ENST00000614259.2:c.9871C>G
|
ENSP00000506251.1:n.9871C>G
|
|
ENST00000680887.1:c.9863C>G
|
ENSP00000505508.1:p.Thr3288Arg
|
|
ENST00000380152.7:c.9863C>G
|
ENSP00000369497.3:p.Thr3288Arg
|
|
ENST00000533776.1:n.451C>G
|
|
|
ENST00000544455.5:c.9863C>G
|
ENSP00000439902.1:p.Thr3288Arg
|
|
NM_000059.3:c.9863C>G , LRG_293t1:c.9863C>G
|
NP_000050.2:p.Thr3288Arg
|
|
XM_011535203.1:c.9863C>G
|
XP_011533505.1:p.Thr3288Arg
|
|
XM_011535204.1:c.9767C>G
|
XP_011533506.1:p.Thr3256Arg
|
|
NM_000059.4:c.9863C>G
MANE Select
|
NP_000050.3:p.Thr3288Arg
|
|