ENST00000470094.2:c.8757T=
|
ENSP00000434898.2:p.Gly2919=
|
|
ENST00000528762.2:c.*124T=
|
ENSP00000433168.2:n.*124T=
|
|
ENST00000530893.7:c.8388T=
|
ENSP00000499438.2:p.Gly2796=
|
|
ENST00000665585.2:c.*319T=
|
ENSP00000499570.2:n.*319T=
|
|
ENST00000666593.2:c.8757T=
|
ENSP00000499256.2:p.Gly2919=
|
|
ENST00000700202.2:c.8757T=
|
ENSP00000514856.2:p.Gly2919=
|
|
ENST00000700202.1:c.1224T=
|
ENSP00000514856.1:p.Gly408=
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|
ENST00000700203.1:n.884T=
|
|
|
ENST00000380152.8:c.8757T=
MANE Select
|
ENSP00000369497.3:p.Gly2919=
|
|
ENST00000544455.6:c.8757T=
|
ENSP00000439902.1:p.Gly2919=
|
|
ENST00000614259.2:c.8765T=
|
ENSP00000506251.1:n.8765T=
|
|
ENST00000665585.1:c.1635T=
|
|
|
ENST00000680887.1:c.8757T=
|
ENSP00000505508.1:p.Gly2919=
|
|
ENST00000380152.7:c.8757T=
|
ENSP00000369497.3:p.Gly2919=
|
|
ENST00000528762.1:c.319T=
|
ENSP00000433168.1:n.319T=
|
|
ENST00000544455.5:c.8757T=
|
ENSP00000439902.1:p.Gly2919=
|
|
NM_000059.3:c.8757T= , LRG_293t1:c.8757T=
|
NP_000050.2:p.Gly2919=
|
|
XM_011535203.1:c.8757T=
|
XP_011533505.1:p.Gly2919=
|
|
XM_011535204.1:c.8661T=
|
XP_011533506.1:p.Gly2887=
|
|
XM_011535205.1:c.8755-431T=
|
XP_011533507.1:n.8755-431T=
|
|
NM_000059.4:c.8757T=
MANE Select
|
NP_000050.3:p.Gly2919=
|
|