ENST00000470094.2:c.*297G>T
|
ENSP00000434898.2:n.*297G>T
|
|
ENST00000528762.2:c.*1141G>T
|
ENSP00000433168.2:n.*1141G>T
|
|
ENST00000530893.7:c.9405G>T
|
ENSP00000499438.2:p.Glu3135Asp
|
|
ENST00000665585.2:c.*1336G>T
|
ENSP00000499570.2:n.*1336G>T
|
|
ENST00000700202.2:c.9723G>T
|
ENSP00000514856.2:p.Glu3241Asp
|
|
ENST00000700202.1:c.2190G>T
|
ENSP00000514856.1:p.Glu730Asp
|
|
ENST00000700203.1:n.1901G>T
|
|
|
ENST00000380152.8:c.9774G>T
MANE Select
|
ENSP00000369497.3:p.Glu3258Asp
|
|
ENST00000544455.6:c.9774G>T
|
ENSP00000439902.1:p.Glu3258Asp
|
|
ENST00000614259.2:c.9782G>T
|
ENSP00000506251.1:n.9782G>T
|
|
ENST00000680887.1:c.9774G>T
|
ENSP00000505508.1:p.Glu3258Asp
|
|
ENST00000380152.7:c.9774G>T
|
ENSP00000369497.3:p.Glu3258Asp
|
|
ENST00000533776.1:n.362G>T
|
|
|
ENST00000544455.5:c.9774G>T
|
ENSP00000439902.1:p.Glu3258Asp
|
|
NM_000059.3:c.9774G>T , LRG_293t1:c.9774G>T
|
NP_000050.2:p.Glu3258Asp
|
|
XM_011535203.1:c.9774G>T
|
XP_011533505.1:p.Glu3258Asp
|
|
XM_011535204.1:c.9678G>T
|
XP_011533506.1:p.Glu3226Asp
|
|
NM_000059.4:c.9774G>T
MANE Select
|
NP_000050.3:p.Glu3258Asp
|
|