ENST00000268314.9:c.990G>C
MANE Select
|
ENSP00000268314.4:p.Glu330Asp
|
|
ENST00000268314.8:c.990G>C
|
ENSP00000268314.4:p.Glu330Asp
|
|
ENST00000408912.7:c.1275G>C
|
ENSP00000386125.3:p.Glu425Asp
|
|
ENST00000457010.6:c.990G>C
|
ENSP00000399561.2:p.Glu330Asp
|
|
ENST00000538189.5:c.498G>C
|
ENSP00000443995.2:p.Glu166Asp
|
|
ENST00000563544.5:c.990G>C
|
ENSP00000456877.1:p.Glu330Asp
|
|
ENST00000564900.1:c.213-235G>C
|
|
|
NM_001105247.1:c.990G>C
|
NP_001098717.1:p.Glu330Asp
|
|
NM_001288767.1:c.1275G>C
|
NP_001275696.1:p.Glu425Asp
|
|
NM_001301820.1:c.1086G>C
|
NP_001288749.1:p.Glu362Asp
|
|
NM_024742.2:c.990G>C
|
NP_079018.1:p.Glu330Asp
|
|
XM_006721091.1:c.1086G>C
|
XP_006721154.1:p.Glu362Asp
|
|
XM_006721091.3:c.1086G>C
|
XP_006721154.1:p.Glu362Asp
|
|
XM_024450448.1:c.1086G>C
|
XP_024306216.1:p.Glu362Asp
|
|
XM_024450449.1:c.1086G>C
|
XP_024306217.1:p.Glu362Asp
|
|
NM_001105247.2:c.990G>C
MANE Select
|
NP_001098717.1:p.Glu330Asp
|
|
NM_001288767.2:c.1275G>C
|
NP_001275696.1:p.Glu425Asp
|
|