ENST00000470094.2:c.8831T>G
|
ENSP00000434898.2:p.Ile2944Ser
|
|
ENST00000528762.2:c.*198T>G
|
ENSP00000433168.2:n.*198T>G
|
|
ENST00000530893.7:c.8462T>G
|
ENSP00000499438.2:p.Ile2821Ser
|
|
ENST00000665585.2:c.*393T>G
|
ENSP00000499570.2:n.*393T>G
|
|
ENST00000666593.2:c.8831T>G
|
ENSP00000499256.2:p.Ile2944Ser
|
|
ENST00000700202.2:c.8831T>G
|
ENSP00000514856.2:p.Ile2944Ser
|
|
ENST00000700202.1:c.1298T>G
|
ENSP00000514856.1:p.Ile433Ser
|
|
ENST00000700203.1:n.958T>G
|
|
|
ENST00000380152.8:c.8831T>G
MANE Select
|
ENSP00000369497.3:p.Ile2944Ser
|
|
ENST00000544455.6:c.8831T>G
|
ENSP00000439902.1:p.Ile2944Ser
|
|
ENST00000614259.2:c.8839T>G
|
ENSP00000506251.1:n.8839T>G
|
|
ENST00000665585.1:c.1709T>G
|
|
|
ENST00000680887.1:c.8831T>G
|
ENSP00000505508.1:p.Ile2944Ser
|
|
ENST00000380152.7:c.8831T>G
|
ENSP00000369497.3:p.Ile2944Ser
|
|
ENST00000528762.1:c.393T>G
|
ENSP00000433168.1:n.393T>G
|
|
ENST00000544455.5:c.8831T>G
|
ENSP00000439902.1:p.Ile2944Ser
|
|
NM_000059.3:c.8831T>G , LRG_293t1:c.8831T>G
|
NP_000050.2:p.Ile2944Ser
|
|
XM_011535203.1:c.8831T>G
|
XP_011533505.1:p.Ile2944Ser
|
|
XM_011535204.1:c.8735T>G
|
XP_011533506.1:p.Ile2912Ser
|
|
XM_011535205.1:c.8755-357T>G
|
XP_011533507.1:n.8755-357T>G
|
|
NM_000059.4:c.8831T>G
MANE Select
|
NP_000050.3:p.Ile2944Ser
|
|