ENST00000470094.2:c.*406C>G
|
ENSP00000434898.2:n.*406C>G
|
|
ENST00000528762.2:c.*1250C>G
|
ENSP00000433168.2:n.*1250C>G
|
|
ENST00000530893.7:c.9514C>G
|
ENSP00000499438.2:p.Gln3172Glu
|
|
ENST00000665585.2:c.*1445C>G
|
ENSP00000499570.2:n.*1445C>G
|
|
ENST00000700202.2:c.9832C>G
|
ENSP00000514856.2:p.Gln3278Glu
|
|
ENST00000700202.1:c.2299C>G
|
ENSP00000514856.1:p.Gln767Glu
|
|
ENST00000700203.1:n.2010C>G
|
|
|
ENST00000380152.8:c.9883C>G
MANE Select
|
ENSP00000369497.3:p.Gln3295Glu
|
|
ENST00000544455.6:c.9883C>G
|
ENSP00000439902.1:p.Gln3295Glu
|
|
ENST00000614259.2:c.9891C>G
|
ENSP00000506251.1:n.9891C>G
|
|
ENST00000680887.1:c.9883C>G
|
ENSP00000505508.1:p.Gln3295Glu
|
|
ENST00000380152.7:c.9883C>G
|
ENSP00000369497.3:p.Gln3295Glu
|
|
ENST00000533776.1:n.471C>G
|
|
|
ENST00000544455.5:c.9883C>G
|
ENSP00000439902.1:p.Gln3295Glu
|
|
NM_000059.3:c.9883C>G , LRG_293t1:c.9883C>G
|
NP_000050.2:p.Gln3295Glu
|
|
XM_011535203.1:c.9883C>G
|
XP_011533505.1:p.Gln3295Glu
|
|
XM_011535204.1:c.9787C>G
|
XP_011533506.1:p.Gln3263Glu
|
|
NM_000059.4:c.9883C>G
MANE Select
|
NP_000050.3:p.Gln3295Glu
|
|