ENST00000470094.2:c.9292T>C
|
ENSP00000434898.2:p.Tyr3098His
|
|
ENST00000528762.2:c.*659T>C
|
ENSP00000433168.2:n.*659T>C
|
|
ENST00000530893.7:c.8923T>C
|
ENSP00000499438.2:p.Tyr2975His
|
|
ENST00000665585.2:c.*854T>C
|
ENSP00000499570.2:n.*854T>C
|
|
ENST00000666593.2:c.*137T>C
|
ENSP00000499256.2:n.*137T>C
|
|
ENST00000700202.2:c.9241T>C
|
ENSP00000514856.2:p.Tyr3081His
|
|
ENST00000700202.1:c.1708T>C
|
ENSP00000514856.1:p.Tyr570His
|
|
ENST00000700203.1:n.1419T>C
|
|
|
ENST00000380152.8:c.9292T>C
MANE Select
|
ENSP00000369497.3:p.Tyr3098His
|
|
ENST00000544455.6:c.9292T>C
|
ENSP00000439902.1:p.Tyr3098His
|
|
ENST00000614259.2:c.9300T>C
|
ENSP00000506251.1:n.9300T>C
|
|
ENST00000665585.1:c.2170T>C
|
|
|
ENST00000666593.1:c.314T>C
|
ENSP00000499256.1:n.314T>C
|
|
ENST00000680887.1:c.9292T>C
|
ENSP00000505508.1:p.Tyr3098His
|
|
ENST00000380152.7:c.9292T>C
|
ENSP00000369497.3:p.Tyr3098His
|
|
ENST00000470094.1:c.249T>C
|
|
|
ENST00000544455.5:c.9292T>C
|
ENSP00000439902.1:p.Tyr3098His
|
|
NM_000059.3:c.9292T>C , LRG_293t1:c.9292T>C
|
NP_000050.2:p.Tyr3098His
|
|
XM_011535203.1:c.9292T>C
|
XP_011533505.1:p.Tyr3098His
|
|
XM_011535204.1:c.9196T>C
|
XP_011533506.1:p.Tyr3066His
|
|
NM_000059.4:c.9292T>C
MANE Select
|
NP_000050.3:p.Tyr3098His
|
|