ENST00000470094.2:c.*436G=
|
ENSP00000434898.2:n.*436G=
|
|
ENST00000528762.2:c.*1280G=
|
ENSP00000433168.2:n.*1280G=
|
|
ENST00000530893.7:c.9544G=
|
ENSP00000499438.2:p.Gly3182=
|
|
ENST00000665585.2:c.*1475G=
|
ENSP00000499570.2:n.*1475G=
|
|
ENST00000700202.2:c.9862G=
|
ENSP00000514856.2:p.Gly3288=
|
|
ENST00000700202.1:c.2329G=
|
ENSP00000514856.1:p.Gly777=
|
|
ENST00000700203.1:n.2040G=
|
|
|
ENST00000380152.8:c.9913G=
MANE Select
|
ENSP00000369497.3:p.Gly3305=
|
|
ENST00000544455.6:c.9913G=
|
ENSP00000439902.1:p.Gly3305=
|
|
ENST00000614259.2:c.9921G=
|
ENSP00000506251.1:n.9921G=
|
|
ENST00000680887.1:c.9913G=
|
ENSP00000505508.1:p.Gly3305=
|
|
ENST00000380152.7:c.9913G=
|
ENSP00000369497.3:p.Gly3305=
|
|
ENST00000533776.1:n.501G=
|
|
|
ENST00000544455.5:c.9913G=
|
ENSP00000439902.1:p.Gly3305=
|
|
NM_000059.3:c.9913G= , LRG_293t1:c.9913G=
|
NP_000050.2:p.Gly3305=
|
|
XM_011535203.1:c.9913G=
|
XP_011533505.1:p.Gly3305=
|
|
XM_011535204.1:c.9817G=
|
XP_011533506.1:p.Gly3273=
|
|
NM_000059.4:c.9913G=
MANE Select
|
NP_000050.3:p.Gly3305=
|
|