ENST00000470094.2:c.*78T>G
|
ENSP00000434898.2:n.*78T>G
|
|
ENST00000528762.2:c.*922T>G
|
ENSP00000433168.2:n.*922T>G
|
|
ENST00000530893.7:c.9186T>G
|
ENSP00000499438.2:p.His3062Gln
|
|
ENST00000665585.2:c.*1117T>G
|
ENSP00000499570.2:n.*1117T>G
|
|
ENST00000700202.2:c.9504T>G
|
ENSP00000514856.2:p.His3168Gln
|
|
ENST00000700202.1:c.1971T>G
|
ENSP00000514856.1:p.His657Gln
|
|
ENST00000700203.1:n.1682T>G
|
|
|
ENST00000380152.8:c.9555T>G
MANE Select
|
ENSP00000369497.3:p.His3185Gln
|
|
ENST00000544455.6:c.9555T>G
|
ENSP00000439902.1:p.His3185Gln
|
|
ENST00000614259.2:c.9563T>G
|
ENSP00000506251.1:n.9563T>G
|
|
ENST00000665585.1:c.2433T>G
|
|
|
ENST00000680887.1:c.9555T>G
|
ENSP00000505508.1:p.His3185Gln
|
|
ENST00000380152.7:c.9555T>G
|
ENSP00000369497.3:p.His3185Gln
|
|
ENST00000470094.1:c.638T>G
|
|
|
ENST00000533776.1:n.143T>G
|
|
|
ENST00000544455.5:c.9555T>G
|
ENSP00000439902.1:p.His3185Gln
|
|
NM_000059.3:c.9555T>G , LRG_293t1:c.9555T>G
|
NP_000050.2:p.His3185Gln
|
|
XM_011535203.1:c.9555T>G
|
XP_011533505.1:p.His3185Gln
|
|
XM_011535204.1:c.9459T>G
|
XP_011533506.1:p.His3153Gln
|
|
NM_000059.4:c.9555T>G
MANE Select
|
NP_000050.3:p.His3185Gln
|
|