ENST00000696717.1:c.7G>A
|
ENSP00000512830.1:p.Glu3Lys
|
|
ENST00000696718.1:c.-249-744G>A
|
ENSP00000512831.1:n.-249-744G>A
|
|
ENST00000696719.1:c.286G>A
|
ENSP00000512832.1:p.Glu96Lys
|
|
ENST00000696720.1:n.466G>A
|
|
|
ENST00000310775.12:c.286G>A
MANE Select
|
ENSP00000310842.8:p.Glu96Lys
|
|
ENST00000674831.1:c.286G>A
|
ENSP00000502474.1:p.Glu96Lys
|
|
ENST00000676003.1:c.286G>A
|
ENSP00000502254.1:p.Glu96Lys
|
|
ENST00000300027.12:c.286G>A
|
ENSP00000300027.8:p.Glu96Lys
|
|
ENST00000310775.11:c.286G>A
|
ENSP00000310842.7:p.Glu96Lys
|
|
ENST00000447611.6:c.286G>A
|
ENSP00000413249.2:p.Glu96Lys
|
|
ENST00000563250.5:c.286G>A
|
ENSP00000457029.1:p.Glu96Lys
|
|
ENST00000564920.5:c.286G>A
|
ENSP00000456552.1:p.Glu96Lys
|
|
ENST00000565255.5:c.286G>A
|
ENSP00000454371.1:p.Glu96Lys
|
|
ENST00000565522.5:n.129+13115G>A
|
|
|
ENST00000567891.5:c.286G>A
|
ENSP00000455735.1:p.Glu96Lys
|
|
ENST00000567996.5:c.286G>A
|
ENSP00000458024.1:p.Glu96Lys
|
|
NM_001113378.1:c.286G>A , LRG_500t1:c.286G>A
|
NP_001106849.1:p.Glu96Lys
|
|
NM_018193.2:c.286G>A
|
NP_060663.2:p.Glu96Lys
|
|
XM_011521756.1:c.286G>A
|
XP_011520058.1:p.Glu96Lys
|
|
XM_011521757.1:c.286G>A
|
XP_011520059.1:p.Glu96Lys
|
|
XM_011521758.1:c.286G>A
|
XP_011520060.1:p.Glu96Lys
|
|
XM_011521759.1:c.286G>A
|
XP_011520061.1:p.Glu96Lys
|
|
XM_011521760.1:c.286G>A
|
XP_011520062.1:p.Glu96Lys
|
|
XM_011521761.1:c.286G>A
|
XP_011520063.1:p.Glu96Lys
|
|
XM_011521762.1:c.286G>A
|
XP_011520064.1:p.Glu96Lys
|
|
XM_011521763.1:c.286G>A
|
XP_011520065.1:p.Glu96Lys
|
|
XM_011521764.1:c.286G>A
|
XP_011520066.1:p.Glu96Lys
|
|
XM_011521765.1:c.7G>A
|
XP_011520067.1:p.Glu3Lys
|
|
XM_011521766.1:c.7G>A
|
XP_011520068.1:p.Glu3Lys
|
|
XM_011521767.1:c.7G>A
|
XP_011520069.1:p.Glu3Lys
|
|
XM_011521768.1:c.286G>A
|
XP_011520070.1:p.Glu96Lys
|
|
XM_011521769.1:c.286G>A
|
XP_011520071.1:p.Glu96Lys
|
|
XM_011521756.2:c.286G>A
|
XP_011520058.1:p.Glu96Lys
|
|
XM_011521757.2:c.286G>A
|
XP_011520059.1:p.Glu96Lys
|
|
XM_011521764.2:c.286G>A
|
XP_011520066.1:p.Glu96Lys
|
|
XM_011521767.2:c.7G>A
|
XP_011520069.1:p.Glu3Lys
|
|
NM_001113378.2:c.286G>A
MANE Select
|
NP_001106849.1:p.Glu96Lys
|
|
NM_001376910.1:c.7G>A
|
NP_001363839.1:p.Glu3Lys
|
|
NM_001376911.1:c.286G>A
|
NP_001363840.1:p.Glu96Lys
|
|
NM_018193.3:c.286G>A
|
NP_060663.2:p.Glu96Lys
|
|