ENST00000350026.11:c.3882T>C
|
ENSP00000055163.8:p.Thr1294=
|
|
ENST00000414678.8:c.3951T>C
|
ENSP00000412835.3:p.Thr1317=
|
|
ENST00000637015.2:c.4170T>C
|
ENSP00000489729.2:p.Thr1390=
|
|
ENST00000346085.10:c.3921T>C
|
ENSP00000344546.5:p.Thr1307=
|
|
ENST00000350026.10:c.3633T>C
|
ENSP00000055163.7:p.Thr1211=
|
|
ENST00000414678.7:c.2199T>C
|
ENSP00000412835.2:p.Thr733=
|
|
ENST00000635849.1:c.1362T>C
|
ENSP00000490948.1:p.Thr454=
|
|
ENST00000635957.1:c.996T>C
|
ENSP00000490385.1:p.Thr332=
|
|
ENST00000636930.2:c.4041T>C
MANE Select
|
ENSP00000490491.2:p.Thr1347=
|
|
ENST00000636940.1:n.2038T>C
|
|
|
ENST00000637015.1:c.1409T>C
|
|
|
ENST00000637568.1:c.1323T>C
|
|
|
ENST00000637741.1:n.707T>C
|
|
|
ENST00000637810.1:c.1383T>C
|
ENSP00000489636.1:p.Thr461=
|
|
ENST00000637904.1:c.1542T>C
|
ENSP00000490550.1:p.Thr514=
|
|
ENST00000647938.1:c.3672T>C
|
ENSP00000498155.1:p.Thr1224=
|
|
ENST00000346085.9:c.3672T>C
|
ENSP00000344546.4:p.Thr1224=
|
|
ENST00000350026.9:c.3633T>C
|
ENSP00000055163.7:p.Thr1211=
|
|
ENST00000414678.6:c.2199T>C
|
ENSP00000412835.2:p.Thr733=
|
|
NM_017519.2:c.3633T>C
|
NP_059989.2:p.Thr1211=
|
|
NM_020732.3:c.3672T>C
|
NP_065783.3:p.Thr1224=
|
|
XM_005267069.3:c.3792T>C
|
XP_005267126.2:p.Thr1264=
|
|
XM_011535984.1:c.2871T>C
|
XP_011534286.1:p.Thr957=
|
|
XM_011535985.1:c.2691T>C
|
XP_011534287.1:p.Thr897=
|
|
XM_011535986.1:c.2451T>C
|
XP_011534288.1:p.Thr817=
|
|
XM_011535987.1:c.2070T>C
|
XP_011534289.1:p.Thr690=
|
|
XM_011535988.1:c.933T>C
|
XP_011534290.1:p.Thr311=
|
|
NM_001346813.1:c.3792T>C
|
NP_001333742.1:p.Thr1264=
|
|
NM_001363725.1:c.1542T>C
|
NP_001350654.1:p.Thr514=
|
|
XM_011535984.2:c.4002T>C
|
XP_011534286.2:p.Thr1334=
|
|
XM_011535988.3:c.933T>C
|
XP_011534290.1:p.Thr311=
|
|
XM_017011103.2:c.3903T>C
|
XP_016866592.1:p.Thr1301=
|
|
XM_017011104.1:c.3873T>C
|
XP_016866593.1:p.Thr1291=
|
|
XM_017011105.2:c.3843T>C
|
XP_016866594.1:p.Thr1281=
|
|
XM_017011106.2:c.3714T>C
|
XP_016866595.1:p.Thr1238=
|
|
XM_017011107.2:c.3693T>C
|
XP_016866596.1:p.Thr1231=
|
|
XR_002956289.1:n.4085T>C
|
|
|
NM_001363725.2:c.1542T>C
|
NP_001350654.1:p.Thr514=
|
|
NM_001371656.1:c.3921T>C
|
NP_001358585.1:p.Thr1307=
|
|
NM_001374820.1:c.3921T>C
|
NP_001361749.1:p.Thr1307=
|
|
NM_001374828.1:c.4041T>C
MANE Select
|
NP_001361757.1:p.Thr1347=
|
|
NM_017519.3:c.3882T>C
|
NP_059989.3:p.Thr1294=
|
|