ENST00000350026.11:c.4228G>T
|
ENSP00000055163.8:p.Glu1410Ter
|
|
ENST00000414678.8:c.4297G>T
|
ENSP00000412835.3:p.Glu1433Ter
|
|
ENST00000637015.2:c.4516G>T
|
ENSP00000489729.2:p.Glu1506Ter
|
|
ENST00000346085.10:c.4267G>T
|
ENSP00000344546.5:p.Glu1423Ter
|
|
ENST00000350026.10:c.3979G>T
|
ENSP00000055163.7:p.Glu1327Ter
|
|
ENST00000414678.7:c.2545G>T
|
ENSP00000412835.2:p.Glu849Ter
|
|
ENST00000635849.1:c.1708G>T
|
ENSP00000490948.1:p.Glu570Ter
|
|
ENST00000635957.1:c.1339G>T
|
ENSP00000490385.1:p.Glu447Ter
|
|
ENST00000636227.1:n.2850G>T
|
|
|
ENST00000636254.1:n.307G>T
|
|
|
ENST00000636930.2:c.4387G>T
MANE Select
|
ENSP00000490491.2:p.Glu1463Ter
|
|
ENST00000636940.1:n.2384G>T
|
|
|
ENST00000637015.1:c.1755G>T
|
|
|
ENST00000637568.1:c.1669G>T
|
|
|
ENST00000637741.1:n.1053G>T
|
|
|
ENST00000637810.1:c.1729G>T
|
ENSP00000489636.1:p.Glu577Ter
|
|
ENST00000637904.1:c.1888G>T
|
ENSP00000490550.1:p.Glu630Ter
|
|
ENST00000647938.1:c.4018G>T
|
ENSP00000498155.1:p.Glu1340Ter
|
|
ENST00000346085.9:c.4018G>T
|
ENSP00000344546.4:p.Glu1340Ter
|
|
ENST00000350026.9:c.3979G>T
|
ENSP00000055163.7:p.Glu1327Ter
|
|
ENST00000414678.6:c.2545G>T
|
ENSP00000412835.2:p.Glu849Ter
|
|
NM_017519.2:c.3979G>T
|
NP_059989.2:p.Glu1327Ter
|
|
NM_020732.3:c.4018G>T
|
NP_065783.3:p.Glu1340Ter
|
|
XM_005267069.3:c.4138G>T
|
XP_005267126.2:p.Glu1380Ter
|
|
XM_011535984.1:c.3217G>T
|
XP_011534286.1:p.Glu1073Ter
|
|
XM_011535985.1:c.3037G>T
|
XP_011534287.1:p.Glu1013Ter
|
|
XM_011535986.1:c.2797G>T
|
XP_011534288.1:p.Glu933Ter
|
|
XM_011535987.1:c.2416G>T
|
XP_011534289.1:p.Glu806Ter
|
|
XM_011535988.1:c.1279G>T
|
XP_011534290.1:p.Glu427Ter
|
|
NM_001346813.1:c.4138G>T
|
NP_001333742.1:p.Glu1380Ter
|
|
NM_001363725.1:c.1888G>T
|
NP_001350654.1:p.Glu630Ter
|
|
XM_011535984.2:c.4348G>T
|
XP_011534286.2:p.Glu1450Ter
|
|
XM_011535988.3:c.1279G>T
|
XP_011534290.1:p.Glu427Ter
|
|
XM_017011103.2:c.4249G>T
|
XP_016866592.1:p.Glu1417Ter
|
|
XM_017011104.1:c.4219G>T
|
XP_016866593.1:p.Glu1407Ter
|
|
XM_017011105.2:c.4189G>T
|
XP_016866594.1:p.Glu1397Ter
|
|
XM_017011106.2:c.4060G>T
|
XP_016866595.1:p.Glu1354Ter
|
|
XM_017011107.2:c.4039G>T
|
XP_016866596.1:p.Glu1347Ter
|
|
XR_002956289.1:n.4427-1890G>T
|
|
|
NM_001363725.2:c.1888G>T
|
NP_001350654.1:p.Glu630Ter
|
|
NM_001371656.1:c.4267G>T
|
NP_001358585.1:p.Glu1423Ter
|
|
NM_001374820.1:c.4267G>T
|
NP_001361749.1:p.Glu1423Ter
|
|
NM_001374828.1:c.4387G>T
MANE Select
|
NP_001361757.1:p.Glu1463Ter
|
|
NM_017519.3:c.4228G>T
|
NP_059989.3:p.Glu1410Ter
|
|