ENST00000350026.11:c.4393C>T
|
ENSP00000055163.8:p.Gln1465Ter
|
|
ENST00000414678.8:c.4462C>T
|
ENSP00000412835.3:p.Gln1488Ter
|
|
ENST00000637015.2:c.4681C>T
|
ENSP00000489729.2:p.Gln1561Ter
|
|
ENST00000346085.10:c.4432C>T
|
ENSP00000344546.5:p.Gln1478Ter
|
|
ENST00000350026.10:c.4144C>T
|
ENSP00000055163.7:p.Gln1382Ter
|
|
ENST00000414678.7:c.2710C>T
|
ENSP00000412835.2:p.Gln904Ter
|
|
ENST00000635849.1:c.1873C>T
|
ENSP00000490948.1:p.Gln625Ter
|
|
ENST00000635957.1:c.1504C>T
|
ENSP00000490385.1:p.Gln502Ter
|
|
ENST00000636227.1:n.3015C>T
|
|
|
ENST00000636254.1:n.472C>T
|
|
|
ENST00000636930.2:c.4552C>T
MANE Select
|
ENSP00000490491.2:p.Gln1518Ter
|
|
ENST00000636940.1:n.2549C>T
|
|
|
ENST00000637015.1:c.1920C>T
|
|
|
ENST00000637568.1:c.1834C>T
|
|
|
ENST00000637741.1:n.1218C>T
|
|
|
ENST00000637810.1:c.1894C>T
|
ENSP00000489636.1:p.Gln632Ter
|
|
ENST00000637904.1:c.2053C>T
|
ENSP00000490550.1:p.Gln685Ter
|
|
ENST00000647938.1:c.4183C>T
|
ENSP00000498155.1:p.Gln1395Ter
|
|
ENST00000346085.9:c.4183C>T
|
ENSP00000344546.4:p.Gln1395Ter
|
|
ENST00000350026.9:c.4144C>T
|
ENSP00000055163.7:p.Gln1382Ter
|
|
ENST00000414678.6:c.2710C>T
|
ENSP00000412835.2:p.Gln904Ter
|
|
NM_017519.2:c.4144C>T
|
NP_059989.2:p.Gln1382Ter
|
|
NM_020732.3:c.4183C>T
|
NP_065783.3:p.Gln1395Ter
|
|
XM_005267069.3:c.4303C>T
|
XP_005267126.2:p.Gln1435Ter
|
|
XM_011535984.1:c.3382C>T
|
XP_011534286.1:p.Gln1128Ter
|
|
XM_011535985.1:c.3202C>T
|
XP_011534287.1:p.Gln1068Ter
|
|
XM_011535986.1:c.2962C>T
|
XP_011534288.1:p.Gln988Ter
|
|
XM_011535987.1:c.2581C>T
|
XP_011534289.1:p.Gln861Ter
|
|
XM_011535988.1:c.1444C>T
|
XP_011534290.1:p.Gln482Ter
|
|
NM_001346813.1:c.4303C>T
|
NP_001333742.1:p.Gln1435Ter
|
|
NM_001363725.1:c.2053C>T
|
NP_001350654.1:p.Gln685Ter
|
|
XM_011535984.2:c.4513C>T
|
XP_011534286.2:p.Gln1505Ter
|
|
XM_011535988.3:c.1444C>T
|
XP_011534290.1:p.Gln482Ter
|
|
XM_017011103.2:c.4414C>T
|
XP_016866592.1:p.Gln1472Ter
|
|
XM_017011104.1:c.4384C>T
|
XP_016866593.1:p.Gln1462Ter
|
|
XM_017011105.2:c.4354C>T
|
XP_016866594.1:p.Gln1452Ter
|
|
XM_017011106.2:c.4225C>T
|
XP_016866595.1:p.Gln1409Ter
|
|
XM_017011107.2:c.4204C>T
|
XP_016866596.1:p.Gln1402Ter
|
|
XR_002956289.1:n.4499C>T
|
|
|
NM_001363725.2:c.2053C>T
|
NP_001350654.1:p.Gln685Ter
|
|
NM_001371656.1:c.4432C>T
|
NP_001358585.1:p.Gln1478Ter
|
|
NM_001374820.1:c.4432C>T
|
NP_001361749.1:p.Gln1478Ter
|
|
NM_001374828.1:c.4552C>T
MANE Select
|
NP_001361757.1:p.Gln1518Ter
|
|
NM_017519.3:c.4393C>T
|
NP_059989.3:p.Gln1465Ter
|
|