ENST00000350026.11:c.4977A>G
|
ENSP00000055163.8:p.Thr1659=
|
|
ENST00000414678.8:c.5046A>G
|
ENSP00000412835.3:p.Thr1682=
|
|
ENST00000637015.2:c.5265A>G
|
ENSP00000489729.2:p.Thr1755=
|
|
ENST00000346085.10:c.5016A>G
|
ENSP00000344546.5:p.Thr1672=
|
|
ENST00000350026.10:c.4728A>G
|
ENSP00000055163.7:p.Thr1576=
|
|
ENST00000414678.7:c.3294A>G
|
ENSP00000412835.2:p.Thr1098=
|
|
ENST00000635849.1:c.2457A>G
|
ENSP00000490948.1:p.Thr819=
|
|
ENST00000635957.1:c.2088A>G
|
ENSP00000490385.1:p.Thr696=
|
|
ENST00000636227.1:n.3599A>G
|
|
|
ENST00000636254.1:n.1056A>G
|
|
|
ENST00000636930.2:c.5136A>G
MANE Select
|
ENSP00000490491.2:p.Thr1712=
|
|
ENST00000636940.1:n.3133A>G
|
|
|
ENST00000637015.1:c.2504A>G
|
|
|
ENST00000637568.1:c.2418A>G
|
|
|
ENST00000637741.1:n.1802A>G
|
|
|
ENST00000637810.1:c.2478A>G
|
ENSP00000489636.1:p.Thr826=
|
|
ENST00000637904.1:c.2637A>G
|
ENSP00000490550.1:p.Thr879=
|
|
ENST00000647938.1:c.4767A>G
|
ENSP00000498155.1:p.Thr1589=
|
|
ENST00000346085.9:c.4767A>G
|
ENSP00000344546.4:p.Thr1589=
|
|
ENST00000350026.9:c.4728A>G
|
ENSP00000055163.7:p.Thr1576=
|
|
ENST00000414678.6:c.3294A>G
|
ENSP00000412835.2:p.Thr1098=
|
|
NM_017519.2:c.4728A>G
|
NP_059989.2:p.Thr1576=
|
|
NM_020732.3:c.4767A>G
|
NP_065783.3:p.Thr1589=
|
|
XM_005267069.3:c.4887A>G
|
XP_005267126.2:p.Thr1629=
|
|
XM_011535984.1:c.3966A>G
|
XP_011534286.1:p.Thr1322=
|
|
XM_011535985.1:c.3786A>G
|
XP_011534287.1:p.Thr1262=
|
|
XM_011535986.1:c.3546A>G
|
XP_011534288.1:p.Thr1182=
|
|
XM_011535987.1:c.3165A>G
|
XP_011534289.1:p.Thr1055=
|
|
XM_011535988.1:c.2028A>G
|
XP_011534290.1:p.Thr676=
|
|
NM_001346813.1:c.4887A>G
|
NP_001333742.1:p.Thr1629=
|
|
NM_001363725.1:c.2637A>G
|
NP_001350654.1:p.Thr879=
|
|
XM_011535984.2:c.5097A>G
|
XP_011534286.2:p.Thr1699=
|
|
XM_011535988.3:c.2028A>G
|
XP_011534290.1:p.Thr676=
|
|
XM_017011103.2:c.4998A>G
|
XP_016866592.1:p.Thr1666=
|
|
XM_017011104.1:c.4968A>G
|
XP_016866593.1:p.Thr1656=
|
|
XM_017011105.2:c.4938A>G
|
XP_016866594.1:p.Thr1646=
|
|
XM_017011106.2:c.4809A>G
|
XP_016866595.1:p.Thr1603=
|
|
XM_017011107.2:c.4788A>G
|
XP_016866596.1:p.Thr1596=
|
|
XR_002956289.1:n.5083A>G
|
|
|
NM_001363725.2:c.2637A>G
|
NP_001350654.1:p.Thr879=
|
|
NM_001371656.1:c.5016A>G
|
NP_001358585.1:p.Thr1672=
|
|
NM_001374820.1:c.5016A>G
|
NP_001361749.1:p.Thr1672=
|
|
NM_001374828.1:c.5136A>G
MANE Select
|
NP_001361757.1:p.Thr1712=
|
|
NM_017519.3:c.4977A>G
|
NP_059989.3:p.Thr1659=
|
|