ENST00000470094.2:c.*508A>C
|
ENSP00000434898.2:n.*508A>C
|
|
ENST00000528762.2:c.*1352A>C
|
ENSP00000433168.2:n.*1352A>C
|
|
ENST00000530893.7:c.9616A>C
|
ENSP00000499438.2:p.Asn3206His
|
|
ENST00000665585.2:c.*1547A>C
|
ENSP00000499570.2:n.*1547A>C
|
|
ENST00000700202.2:c.9934A>C
|
ENSP00000514856.2:p.Asn3312His
|
|
ENST00000700202.1:c.2401A>C
|
ENSP00000514856.1:p.Asn801His
|
|
ENST00000700203.1:n.2112A>C
|
|
|
ENST00000380152.8:c.9985A>C
MANE Select
|
ENSP00000369497.3:p.Asn3329His
|
|
ENST00000544455.6:c.9985A>C
|
ENSP00000439902.1:p.Asn3329His
|
|
ENST00000614259.2:c.9993A>C
|
ENSP00000506251.1:n.9993A>C
|
|
ENST00000680887.1:c.9985A>C
|
ENSP00000505508.1:p.Asn3329His
|
|
ENST00000380152.7:c.9985A>C
|
ENSP00000369497.3:p.Asn3329His
|
|
ENST00000544455.5:c.9985A>C
|
ENSP00000439902.1:p.Asn3329His
|
|
NM_000059.3:c.9985A>C , LRG_293t1:c.9985A>C
|
NP_000050.2:p.Asn3329His
|
|
XM_011535203.1:c.9985A>C
|
XP_011533505.1:p.Asn3329His
|
|
XM_011535204.1:c.9889A>C
|
XP_011533506.1:p.Asn3297His
|
|
NM_000059.4:c.9985A>C
MANE Select
|
NP_000050.3:p.Asn3329His
|
|