ENST00000470094.2:c.7906T>G
|
ENSP00000434898.2:p.Cys2636Gly
|
|
ENST00000528762.2:c.7906T>G
|
ENSP00000433168.2:p.Cys2636Gly
|
|
ENST00000530893.7:c.7537T>G
|
ENSP00000499438.2:p.Cys2513Gly
|
|
ENST00000665585.2:c.7906T>G
|
ENSP00000499570.2:p.Cys2636Gly
|
|
ENST00000666593.2:c.7906T>G
|
ENSP00000499256.2:p.Cys2636Gly
|
|
ENST00000700202.2:c.7906T>G
|
ENSP00000514856.2:p.Cys2636Gly
|
|
ENST00000700202.1:c.373T>G
|
ENSP00000514856.1:p.Cys125Gly
|
|
ENST00000380152.8:c.7906T>G
MANE Select
|
ENSP00000369497.3:p.Cys2636Gly
|
|
ENST00000544455.6:c.7906T>G
|
ENSP00000439902.1:p.Cys2636Gly
|
|
ENST00000614259.2:c.7914T>G
|
ENSP00000506251.1:p.Asn2638Lys
|
|
ENST00000665585.1:c.471T>G
|
|
|
ENST00000680887.1:c.7906T>G
|
ENSP00000505508.1:p.Cys2636Gly
|
|
ENST00000380152.7:c.7906T>G
|
ENSP00000369497.3:p.Cys2636Gly
|
|
ENST00000544455.5:c.7906T>G
|
ENSP00000439902.1:p.Cys2636Gly
|
|
ENST00000614259.1:n.7914T>G
|
|
|
NM_000059.3:c.7906T>G , LRG_293t1:c.7906T>G
|
NP_000050.2:p.Cys2636Gly
|
|
XM_011535203.1:c.7906T>G
|
XP_011533505.1:p.Cys2636Gly
|
|
XM_011535204.1:c.7810T>G
|
XP_011533506.1:p.Cys2604Gly
|
|
XM_011535205.1:c.7906T>G
|
XP_011533507.1:p.Cys2636Gly
|
|
NM_000059.4:c.7906T>G
MANE Select
|
NP_000050.3:p.Cys2636Gly
|
|