ENST00000350026.11:c.4735G>T
|
ENSP00000055163.8:p.Glu1579Ter
|
|
ENST00000414678.8:c.4804G>T
|
ENSP00000412835.3:p.Glu1602Ter
|
|
ENST00000637015.2:c.5023G>T
|
ENSP00000489729.2:p.Glu1675Ter
|
|
ENST00000346085.10:c.4774G>T
|
ENSP00000344546.5:p.Glu1592Ter
|
|
ENST00000350026.10:c.4486G>T
|
ENSP00000055163.7:p.Glu1496Ter
|
|
ENST00000414678.7:c.3052G>T
|
ENSP00000412835.2:p.Glu1018Ter
|
|
ENST00000635849.1:c.2215G>T
|
ENSP00000490948.1:p.Glu739Ter
|
|
ENST00000635957.1:c.1846G>T
|
ENSP00000490385.1:p.Glu616Ter
|
|
ENST00000636227.1:n.3357G>T
|
|
|
ENST00000636254.1:n.814G>T
|
|
|
ENST00000636930.2:c.4894G>T
MANE Select
|
ENSP00000490491.2:p.Glu1632Ter
|
|
ENST00000636940.1:n.2891G>T
|
|
|
ENST00000637015.1:c.2262G>T
|
|
|
ENST00000637568.1:c.2176G>T
|
|
|
ENST00000637741.1:n.1560G>T
|
|
|
ENST00000637810.1:c.2236G>T
|
ENSP00000489636.1:p.Glu746Ter
|
|
ENST00000637904.1:c.2395G>T
|
ENSP00000490550.1:p.Glu799Ter
|
|
ENST00000647938.1:c.4525G>T
|
ENSP00000498155.1:p.Glu1509Ter
|
|
ENST00000346085.9:c.4525G>T
|
ENSP00000344546.4:p.Glu1509Ter
|
|
ENST00000350026.9:c.4486G>T
|
ENSP00000055163.7:p.Glu1496Ter
|
|
ENST00000414678.6:c.3052G>T
|
ENSP00000412835.2:p.Glu1018Ter
|
|
NM_017519.2:c.4486G>T
|
NP_059989.2:p.Glu1496Ter
|
|
NM_020732.3:c.4525G>T
|
NP_065783.3:p.Glu1509Ter
|
|
XM_005267069.3:c.4645G>T
|
XP_005267126.2:p.Glu1549Ter
|
|
XM_011535984.1:c.3724G>T
|
XP_011534286.1:p.Glu1242Ter
|
|
XM_011535985.1:c.3544G>T
|
XP_011534287.1:p.Glu1182Ter
|
|
XM_011535986.1:c.3304G>T
|
XP_011534288.1:p.Glu1102Ter
|
|
XM_011535987.1:c.2923G>T
|
XP_011534289.1:p.Glu975Ter
|
|
XM_011535988.1:c.1786G>T
|
XP_011534290.1:p.Glu596Ter
|
|
NM_001346813.1:c.4645G>T
|
NP_001333742.1:p.Glu1549Ter
|
|
NM_001363725.1:c.2395G>T
|
NP_001350654.1:p.Glu799Ter
|
|
XM_011535984.2:c.4855G>T
|
XP_011534286.2:p.Glu1619Ter
|
|
XM_011535988.3:c.1786G>T
|
XP_011534290.1:p.Glu596Ter
|
|
XM_017011103.2:c.4756G>T
|
XP_016866592.1:p.Glu1586Ter
|
|
XM_017011104.1:c.4726G>T
|
XP_016866593.1:p.Glu1576Ter
|
|
XM_017011105.2:c.4696G>T
|
XP_016866594.1:p.Glu1566Ter
|
|
XM_017011106.2:c.4567G>T
|
XP_016866595.1:p.Glu1523Ter
|
|
XM_017011107.2:c.4546G>T
|
XP_016866596.1:p.Glu1516Ter
|
|
XR_002956289.1:n.4841G>T
|
|
|
NM_001363725.2:c.2395G>T
|
NP_001350654.1:p.Glu799Ter
|
|
NM_001371656.1:c.4774G>T
|
NP_001358585.1:p.Glu1592Ter
|
|
NM_001374820.1:c.4774G>T
|
NP_001361749.1:p.Glu1592Ter
|
|
NM_001374828.1:c.4894G>T
MANE Select
|
NP_001361757.1:p.Glu1632Ter
|
|
NM_017519.3:c.4735G>T
|
NP_059989.3:p.Glu1579Ter
|
|