|
ENST00000350026.11:c.4312C>T
|
ENSP00000055163.8:p.Gln1438Ter
|
|
|
ENST00000414678.8:c.4381C>T
|
ENSP00000412835.3:p.Gln1461Ter
|
|
|
ENST00000637015.2:c.4600C>T
|
ENSP00000489729.2:p.Gln1534Ter
|
|
|
ENST00000346085.10:c.4351C>T
|
ENSP00000344546.5:p.Gln1451Ter
|
|
|
ENST00000350026.10:c.4063C>T
|
ENSP00000055163.7:p.Gln1355Ter
|
|
|
ENST00000414678.7:c.2629C>T
|
ENSP00000412835.2:p.Gln877Ter
|
|
|
ENST00000635849.1:c.1792C>T
|
ENSP00000490948.1:p.Gln598Ter
|
|
|
ENST00000635957.1:c.1423C>T
|
ENSP00000490385.1:p.Gln475Ter
|
|
|
ENST00000636227.1:n.2934C>T
|
|
|
|
ENST00000636254.1:n.391C>T
|
|
|
|
ENST00000636930.2:c.4471C>T
MANE Select
|
ENSP00000490491.2:p.Gln1491Ter
|
|
|
ENST00000636940.1:n.2468C>T
|
|
|
|
ENST00000637015.1:c.1839C>T
|
|
|
|
ENST00000637568.1:c.1753C>T
|
|
|
|
ENST00000637741.1:n.1137C>T
|
|
|
|
ENST00000637810.1:c.1813C>T
|
ENSP00000489636.1:p.Gln605Ter
|
|
|
ENST00000637904.1:c.1972C>T
|
ENSP00000490550.1:p.Gln658Ter
|
|
|
ENST00000647938.1:c.4102C>T
|
ENSP00000498155.1:p.Gln1368Ter
|
|
|
ENST00000346085.9:c.4102C>T
|
ENSP00000344546.4:p.Gln1368Ter
|
|
|
ENST00000350026.9:c.4063C>T
|
ENSP00000055163.7:p.Gln1355Ter
|
|
|
ENST00000414678.6:c.2629C>T
|
ENSP00000412835.2:p.Gln877Ter
|
|
|
NM_017519.2:c.4063C>T
|
NP_059989.2:p.Gln1355Ter
|
|
|
NM_020732.3:c.4102C>T
|
NP_065783.3:p.Gln1368Ter
|
|
|
XM_005267069.3:c.4222C>T
|
XP_005267126.2:p.Gln1408Ter
|
|
|
XM_011535984.1:c.3301C>T
|
XP_011534286.1:p.Gln1101Ter
|
|
|
XM_011535985.1:c.3121C>T
|
XP_011534287.1:p.Gln1041Ter
|
|
|
XM_011535986.1:c.2881C>T
|
XP_011534288.1:p.Gln961Ter
|
|
|
XM_011535987.1:c.2500C>T
|
XP_011534289.1:p.Gln834Ter
|
|
|
XM_011535988.1:c.1363C>T
|
XP_011534290.1:p.Gln455Ter
|
|
|
NM_001346813.1:c.4222C>T
|
NP_001333742.1:p.Gln1408Ter
|
|
|
NM_001363725.1:c.1972C>T
|
NP_001350654.1:p.Gln658Ter
|
|
|
XM_011535984.2:c.4432C>T
|
XP_011534286.2:p.Gln1478Ter
|
|
|
XM_011535988.3:c.1363C>T
|
XP_011534290.1:p.Gln455Ter
|
|
|
XM_017011103.2:c.4333C>T
|
XP_016866592.1:p.Gln1445Ter
|
|
|
XM_017011104.1:c.4303C>T
|
XP_016866593.1:p.Gln1435Ter
|
|
|
XM_017011105.2:c.4273C>T
|
XP_016866594.1:p.Gln1425Ter
|
|
|
XM_017011106.2:c.4144C>T
|
XP_016866595.1:p.Gln1382Ter
|
|
|
XM_017011107.2:c.4123C>T
|
XP_016866596.1:p.Gln1375Ter
|
|
|
XR_002956289.1:n.4427-1806C>T
|
|
|
|
NM_001363725.2:c.1972C>T
|
NP_001350654.1:p.Gln658Ter
|
|
|
NM_001371656.1:c.4351C>T
|
NP_001358585.1:p.Gln1451Ter
|
|
|
NM_001374820.1:c.4351C>T
|
NP_001361749.1:p.Gln1451Ter
|
|
|
NM_001374828.1:c.4471C>T
MANE Select
|
NP_001361757.1:p.Gln1491Ter
|
|
|
NM_017519.3:c.4312C>T
|
NP_059989.3:p.Gln1438Ter
|
|
