ENST00000350026.11:c.5455G=
|
ENSP00000055163.8:p.Glu1819=
|
|
ENST00000414678.8:c.5524G=
|
ENSP00000412835.3:p.Glu1842=
|
|
ENST00000637015.2:c.5743G=
|
ENSP00000489729.2:p.Glu1915=
|
|
ENST00000346085.10:c.5494G=
|
ENSP00000344546.5:p.Glu1832=
|
|
ENST00000350026.10:c.5206G=
|
ENSP00000055163.7:p.Glu1736=
|
|
ENST00000414678.7:c.3772G=
|
ENSP00000412835.2:p.Glu1258=
|
|
ENST00000635849.1:c.2935G=
|
ENSP00000490948.1:p.Glu979=
|
|
ENST00000635957.1:c.2566G=
|
ENSP00000490385.1:p.Glu856=
|
|
ENST00000636227.1:n.4077G=
|
|
|
ENST00000636254.1:n.1534G=
|
|
|
ENST00000636930.2:c.5614G=
MANE Select
|
ENSP00000490491.2:p.Glu1872=
|
|
ENST00000636940.1:n.3611G=
|
|
|
ENST00000637015.1:c.2982G=
|
|
|
ENST00000637568.1:c.2896G=
|
|
|
ENST00000637741.1:n.2280G=
|
|
|
ENST00000637810.1:c.2956G=
|
ENSP00000489636.1:p.Glu986=
|
|
ENST00000637904.1:c.3115G=
|
ENSP00000490550.1:p.Glu1039=
|
|
ENST00000637933.1:n.2729G=
|
|
|
ENST00000647938.1:c.5245G=
|
ENSP00000498155.1:p.Glu1749=
|
|
ENST00000346085.9:c.5245G=
|
ENSP00000344546.4:p.Glu1749=
|
|
ENST00000350026.9:c.5206G=
|
ENSP00000055163.7:p.Glu1736=
|
|
ENST00000414678.6:c.3772G=
|
ENSP00000412835.2:p.Glu1258=
|
|
NM_017519.2:c.5206G=
|
NP_059989.2:p.Glu1736=
|
|
NM_020732.3:c.5245G=
|
NP_065783.3:p.Glu1749=
|
|
XM_005267069.3:c.5365G=
|
XP_005267126.2:p.Glu1789=
|
|
XM_011535984.1:c.4444G=
|
XP_011534286.1:p.Glu1482=
|
|
XM_011535985.1:c.4264G=
|
XP_011534287.1:p.Glu1422=
|
|
XM_011535986.1:c.4024G=
|
XP_011534288.1:p.Glu1342=
|
|
XM_011535987.1:c.3643G=
|
XP_011534289.1:p.Glu1215=
|
|
XM_011535988.1:c.2506G=
|
XP_011534290.1:p.Glu836=
|
|
NM_001346813.1:c.5365G=
|
NP_001333742.1:p.Glu1789=
|
|
NM_001363725.1:c.3115G=
|
NP_001350654.1:p.Glu1039=
|
|
XM_011535984.2:c.5575G=
|
XP_011534286.2:p.Glu1859=
|
|
XM_011535988.3:c.2506G=
|
XP_011534290.1:p.Glu836=
|
|
XM_017011103.2:c.5476G=
|
XP_016866592.1:p.Glu1826=
|
|
XM_017011104.1:c.5446G=
|
XP_016866593.1:p.Glu1816=
|
|
XM_017011105.2:c.5416G=
|
XP_016866594.1:p.Glu1806=
|
|
XM_017011106.2:c.5287G=
|
XP_016866595.1:p.Glu1763=
|
|
XM_017011107.2:c.5266G=
|
XP_016866596.1:p.Glu1756=
|
|
XR_002956289.1:n.5561G=
|
|
|
NM_001363725.2:c.3115G=
|
NP_001350654.1:p.Glu1039=
|
|
NM_001371656.1:c.5494G=
|
NP_001358585.1:p.Glu1832=
|
|
NM_001374820.1:c.5494G=
|
NP_001361749.1:p.Glu1832=
|
|
NM_001374828.1:c.5614G=
MANE Select
|
NP_001361757.1:p.Glu1872=
|
|
NM_017519.3:c.5455G=
|
NP_059989.3:p.Glu1819=
|
|