ENST00000350026.11:c.3975T>C
|
ENSP00000055163.8:p.Thr1325=
|
|
ENST00000414678.8:c.4044T>C
|
ENSP00000412835.3:p.Thr1348=
|
|
ENST00000637015.2:c.4263T>C
|
ENSP00000489729.2:p.Thr1421=
|
|
ENST00000346085.10:c.4014T>C
|
ENSP00000344546.5:p.Thr1338=
|
|
ENST00000350026.10:c.3726T>C
|
ENSP00000055163.7:p.Thr1242=
|
|
ENST00000414678.7:c.2292T>C
|
ENSP00000412835.2:p.Thr764=
|
|
ENST00000635849.1:c.1455T>C
|
ENSP00000490948.1:p.Thr485=
|
|
ENST00000635957.1:c.1086T>C
|
ENSP00000490385.1:p.Thr362=
|
|
ENST00000636930.2:c.4134T>C
MANE Select
|
ENSP00000490491.2:p.Thr1378=
|
|
ENST00000636940.1:n.2131T>C
|
|
|
ENST00000637015.1:c.1502T>C
|
|
|
ENST00000637568.1:c.1416T>C
|
|
|
ENST00000637741.1:n.800T>C
|
|
|
ENST00000637810.1:c.1476T>C
|
ENSP00000489636.1:p.Thr492=
|
|
ENST00000637904.1:c.1635T>C
|
ENSP00000490550.1:p.Thr545=
|
|
ENST00000647938.1:c.3765T>C
|
ENSP00000498155.1:p.Thr1255=
|
|
ENST00000346085.9:c.3765T>C
|
ENSP00000344546.4:p.Thr1255=
|
|
ENST00000350026.9:c.3726T>C
|
ENSP00000055163.7:p.Thr1242=
|
|
ENST00000414678.6:c.2292T>C
|
ENSP00000412835.2:p.Thr764=
|
|
NM_017519.2:c.3726T>C
|
NP_059989.2:p.Thr1242=
|
|
NM_020732.3:c.3765T>C
|
NP_065783.3:p.Thr1255=
|
|
XM_005267069.3:c.3885T>C
|
XP_005267126.2:p.Thr1295=
|
|
XM_011535984.1:c.2964T>C
|
XP_011534286.1:p.Thr988=
|
|
XM_011535985.1:c.2784T>C
|
XP_011534287.1:p.Thr928=
|
|
XM_011535986.1:c.2544T>C
|
XP_011534288.1:p.Thr848=
|
|
XM_011535987.1:c.2163T>C
|
XP_011534289.1:p.Thr721=
|
|
XM_011535988.1:c.1026T>C
|
XP_011534290.1:p.Thr342=
|
|
NM_001346813.1:c.3885T>C
|
NP_001333742.1:p.Thr1295=
|
|
NM_001363725.1:c.1635T>C
|
NP_001350654.1:p.Thr545=
|
|
XM_011535984.2:c.4095T>C
|
XP_011534286.2:p.Thr1365=
|
|
XM_011535988.3:c.1026T>C
|
XP_011534290.1:p.Thr342=
|
|
XM_017011103.2:c.3996T>C
|
XP_016866592.1:p.Thr1332=
|
|
XM_017011104.1:c.3966T>C
|
XP_016866593.1:p.Thr1322=
|
|
XM_017011105.2:c.3936T>C
|
XP_016866594.1:p.Thr1312=
|
|
XM_017011106.2:c.3807T>C
|
XP_016866595.1:p.Thr1269=
|
|
XM_017011107.2:c.3786T>C
|
XP_016866596.1:p.Thr1262=
|
|
XR_002956289.1:n.4178T>C
|
|
|
NM_001363725.2:c.1635T>C
|
NP_001350654.1:p.Thr545=
|
|
NM_001371656.1:c.4014T>C
|
NP_001358585.1:p.Thr1338=
|
|
NM_001374820.1:c.4014T>C
|
NP_001361749.1:p.Thr1338=
|
|
NM_001374828.1:c.4134T>C
MANE Select
|
NP_001361757.1:p.Thr1378=
|
|
NM_017519.3:c.3975T>C
|
NP_059989.3:p.Thr1325=
|
|