ENST00000470094.2:c.*420G=
|
ENSP00000434898.2:n.*420G=
|
|
ENST00000528762.2:c.*1264G=
|
ENSP00000433168.2:n.*1264G=
|
|
ENST00000530893.7:c.9528G=
|
ENSP00000499438.2:p.Gln3176=
|
|
ENST00000665585.2:c.*1459G=
|
ENSP00000499570.2:n.*1459G=
|
|
ENST00000700202.2:c.9846G=
|
ENSP00000514856.2:p.Gln3282=
|
|
ENST00000700202.1:c.2313G=
|
ENSP00000514856.1:p.Gln771=
|
|
ENST00000700203.1:n.2024G=
|
|
|
ENST00000380152.8:c.9897G=
MANE Select
|
ENSP00000369497.3:p.Gln3299=
|
|
ENST00000544455.6:c.9897G=
|
ENSP00000439902.1:p.Gln3299=
|
|
ENST00000614259.2:c.9905G=
|
ENSP00000506251.1:n.9905G=
|
|
ENST00000680887.1:c.9897G=
|
ENSP00000505508.1:p.Gln3299=
|
|
ENST00000380152.7:c.9897G=
|
ENSP00000369497.3:p.Gln3299=
|
|
ENST00000533776.1:n.485G=
|
|
|
ENST00000544455.5:c.9897G=
|
ENSP00000439902.1:p.Gln3299=
|
|
NM_000059.3:c.9897G= , LRG_293t1:c.9897G=
|
NP_000050.2:p.Gln3299=
|
|
XM_011535203.1:c.9897G=
|
XP_011533505.1:p.Gln3299=
|
|
XM_011535204.1:c.9801G=
|
XP_011533506.1:p.Gln3267=
|
|
NM_000059.4:c.9897G=
MANE Select
|
NP_000050.3:p.Gln3299=
|
|