ENST00000470094.2:c.*414A>G
|
ENSP00000434898.2:n.*414A>G
|
|
ENST00000528762.2:c.*1258A>G
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ENSP00000433168.2:n.*1258A>G
|
|
ENST00000530893.7:c.9522A>G
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ENSP00000499438.2:p.Ala3174=
|
|
ENST00000665585.2:c.*1453A>G
|
ENSP00000499570.2:n.*1453A>G
|
|
ENST00000700202.2:c.9840A>G
|
ENSP00000514856.2:p.Ala3280=
|
|
ENST00000700202.1:c.2307A>G
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ENSP00000514856.1:p.Ala769=
|
|
ENST00000700203.1:n.2018A>G
|
|
|
ENST00000380152.8:c.9891A>G
MANE Select
|
ENSP00000369497.3:p.Ala3297=
|
|
ENST00000544455.6:c.9891A>G
|
ENSP00000439902.1:p.Ala3297=
|
|
ENST00000614259.2:c.9899A>G
|
ENSP00000506251.1:n.9899A>G
|
|
ENST00000680887.1:c.9891A>G
|
ENSP00000505508.1:p.Ala3297=
|
|
ENST00000380152.7:c.9891A>G
|
ENSP00000369497.3:p.Ala3297=
|
|
ENST00000533776.1:n.479A>G
|
|
|
ENST00000544455.5:c.9891A>G
|
ENSP00000439902.1:p.Ala3297=
|
|
NM_000059.3:c.9891A>G , LRG_293t1:c.9891A>G
|
NP_000050.2:p.Ala3297=
|
|
XM_011535203.1:c.9891A>G
|
XP_011533505.1:p.Ala3297=
|
|
XM_011535204.1:c.9795A>G
|
XP_011533506.1:p.Ala3265=
|
|
NM_000059.4:c.9891A>G
MANE Select
|
NP_000050.3:p.Ala3297=
|
|