ENST00000350026.11:c.4698A>G
|
ENSP00000055163.8:p.Thr1566=
|
|
ENST00000414678.8:c.4767A>G
|
ENSP00000412835.3:p.Thr1589=
|
|
ENST00000637015.2:c.4986A>G
|
ENSP00000489729.2:p.Thr1662=
|
|
ENST00000346085.10:c.4737A>G
|
ENSP00000344546.5:p.Thr1579=
|
|
ENST00000350026.10:c.4449A>G
|
ENSP00000055163.7:p.Thr1483=
|
|
ENST00000414678.7:c.3015A>G
|
ENSP00000412835.2:p.Thr1005=
|
|
ENST00000635849.1:c.2178A>G
|
ENSP00000490948.1:p.Thr726=
|
|
ENST00000635957.1:c.1809A>G
|
ENSP00000490385.1:p.Thr603=
|
|
ENST00000636227.1:n.3320A>G
|
|
|
ENST00000636254.1:n.777A>G
|
|
|
ENST00000636930.2:c.4857A>G
MANE Select
|
ENSP00000490491.2:p.Thr1619=
|
|
ENST00000636940.1:n.2854A>G
|
|
|
ENST00000637015.1:c.2225A>G
|
|
|
ENST00000637568.1:c.2139A>G
|
|
|
ENST00000637741.1:n.1523A>G
|
|
|
ENST00000637810.1:c.2199A>G
|
ENSP00000489636.1:p.Thr733=
|
|
ENST00000637904.1:c.2358A>G
|
ENSP00000490550.1:p.Thr786=
|
|
ENST00000647938.1:c.4488A>G
|
ENSP00000498155.1:p.Thr1496=
|
|
ENST00000346085.9:c.4488A>G
|
ENSP00000344546.4:p.Thr1496=
|
|
ENST00000350026.9:c.4449A>G
|
ENSP00000055163.7:p.Thr1483=
|
|
ENST00000414678.6:c.3015A>G
|
ENSP00000412835.2:p.Thr1005=
|
|
NM_017519.2:c.4449A>G
|
NP_059989.2:p.Thr1483=
|
|
NM_020732.3:c.4488A>G
|
NP_065783.3:p.Thr1496=
|
|
XM_005267069.3:c.4608A>G
|
XP_005267126.2:p.Thr1536=
|
|
XM_011535984.1:c.3687A>G
|
XP_011534286.1:p.Thr1229=
|
|
XM_011535985.1:c.3507A>G
|
XP_011534287.1:p.Thr1169=
|
|
XM_011535986.1:c.3267A>G
|
XP_011534288.1:p.Thr1089=
|
|
XM_011535987.1:c.2886A>G
|
XP_011534289.1:p.Thr962=
|
|
XM_011535988.1:c.1749A>G
|
XP_011534290.1:p.Thr583=
|
|
NM_001346813.1:c.4608A>G
|
NP_001333742.1:p.Thr1536=
|
|
NM_001363725.1:c.2358A>G
|
NP_001350654.1:p.Thr786=
|
|
XM_011535984.2:c.4818A>G
|
XP_011534286.2:p.Thr1606=
|
|
XM_011535988.3:c.1749A>G
|
XP_011534290.1:p.Thr583=
|
|
XM_017011103.2:c.4719A>G
|
XP_016866592.1:p.Thr1573=
|
|
XM_017011104.1:c.4689A>G
|
XP_016866593.1:p.Thr1563=
|
|
XM_017011105.2:c.4659A>G
|
XP_016866594.1:p.Thr1553=
|
|
XM_017011106.2:c.4530A>G
|
XP_016866595.1:p.Thr1510=
|
|
XM_017011107.2:c.4509A>G
|
XP_016866596.1:p.Thr1503=
|
|
XR_002956289.1:n.4804A>G
|
|
|
NM_001363725.2:c.2358A>G
|
NP_001350654.1:p.Thr786=
|
|
NM_001371656.1:c.4737A>G
|
NP_001358585.1:p.Thr1579=
|
|
NM_001374820.1:c.4737A>G
|
NP_001361749.1:p.Thr1579=
|
|
NM_001374828.1:c.4857A>G
MANE Select
|
NP_001361757.1:p.Thr1619=
|
|
NM_017519.3:c.4698A>G
|
NP_059989.3:p.Thr1566=
|
|