ENST00000470094.2:c.9236T>G
|
ENSP00000434898.2:p.Val3079Gly
|
|
ENST00000528762.2:c.*603T>G
|
ENSP00000433168.2:n.*603T>G
|
|
ENST00000530893.7:c.8867T>G
|
ENSP00000499438.2:p.Val2956Gly
|
|
ENST00000665585.2:c.*798T>G
|
ENSP00000499570.2:n.*798T>G
|
|
ENST00000666593.2:c.9236T>G
|
ENSP00000499256.2:p.Val3079Gly
|
|
ENST00000700202.2:c.9185T>G
|
ENSP00000514856.2:p.Val3062Gly
|
|
ENST00000700202.1:c.1652T>G
|
ENSP00000514856.1:p.Val551Gly
|
|
ENST00000700203.1:n.1363T>G
|
|
|
ENST00000380152.8:c.9236T>G
MANE Select
|
ENSP00000369497.3:p.Val3079Gly
|
|
ENST00000544455.6:c.9236T>G
|
ENSP00000439902.1:p.Val3079Gly
|
|
ENST00000614259.2:c.9244T>G
|
ENSP00000506251.1:n.9244T>G
|
|
ENST00000665585.1:c.2114T>G
|
|
|
ENST00000666593.1:c.119T>G
|
ENSP00000499256.1:p.Val40Gly
|
|
ENST00000680887.1:c.9236T>G
|
ENSP00000505508.1:p.Val3079Gly
|
|
ENST00000380152.7:c.9236T>G
|
ENSP00000369497.3:p.Val3079Gly
|
|
ENST00000470094.1:c.193T>G
|
|
|
ENST00000544455.5:c.9236T>G
|
ENSP00000439902.1:p.Val3079Gly
|
|
NM_000059.3:c.9236T>G , LRG_293t1:c.9236T>G
|
NP_000050.2:p.Val3079Gly
|
|
XM_011535203.1:c.9236T>G
|
XP_011533505.1:p.Val3079Gly
|
|
XM_011535204.1:c.9140T>G
|
XP_011533506.1:p.Val3047Gly
|
|
NM_000059.4:c.9236T>G
MANE Select
|
NP_000050.3:p.Val3079Gly
|
|