ENST00000470094.2:c.9293A>G
|
ENSP00000434898.2:p.Tyr3098Cys
|
|
ENST00000528762.2:c.*660A>G
|
ENSP00000433168.2:n.*660A>G
|
|
ENST00000530893.7:c.8924A>G
|
ENSP00000499438.2:p.Tyr2975Cys
|
|
ENST00000665585.2:c.*855A>G
|
ENSP00000499570.2:n.*855A>G
|
|
ENST00000666593.2:c.*138A>G
|
ENSP00000499256.2:n.*138A>G
|
|
ENST00000700202.2:c.9242A>G
|
ENSP00000514856.2:p.Tyr3081Cys
|
|
ENST00000700202.1:c.1709A>G
|
ENSP00000514856.1:p.Tyr570Cys
|
|
ENST00000700203.1:n.1420A>G
|
|
|
ENST00000380152.8:c.9293A>G
MANE Select
|
ENSP00000369497.3:p.Tyr3098Cys
|
|
ENST00000544455.6:c.9293A>G
|
ENSP00000439902.1:p.Tyr3098Cys
|
|
ENST00000614259.2:c.9301A>G
|
ENSP00000506251.1:n.9301A>G
|
|
ENST00000665585.1:c.2171A>G
|
|
|
ENST00000666593.1:c.315A>G
|
ENSP00000499256.1:n.315A>G
|
|
ENST00000680887.1:c.9293A>G
|
ENSP00000505508.1:p.Tyr3098Cys
|
|
ENST00000380152.7:c.9293A>G
|
ENSP00000369497.3:p.Tyr3098Cys
|
|
ENST00000470094.1:c.250A>G
|
|
|
ENST00000544455.5:c.9293A>G
|
ENSP00000439902.1:p.Tyr3098Cys
|
|
NM_000059.3:c.9293A>G , LRG_293t1:c.9293A>G
|
NP_000050.2:p.Tyr3098Cys
|
|
XM_011535203.1:c.9293A>G
|
XP_011533505.1:p.Tyr3098Cys
|
|
XM_011535204.1:c.9197A>G
|
XP_011533506.1:p.Tyr3066Cys
|
|
NM_000059.4:c.9293A>G
MANE Select
|
NP_000050.3:p.Tyr3098Cys
|
|