ENST00000350026.11:c.3792C>T
|
ENSP00000055163.8:p.Thr1264=
|
|
ENST00000414678.8:c.3861C>T
|
ENSP00000412835.3:p.Thr1287=
|
|
ENST00000637015.2:c.4080C>T
|
ENSP00000489729.2:p.Thr1360=
|
|
ENST00000346085.10:c.3831C>T
|
ENSP00000344546.5:p.Thr1277=
|
|
ENST00000350026.10:c.3543C>T
|
ENSP00000055163.7:p.Thr1181=
|
|
ENST00000414678.7:c.2109C>T
|
ENSP00000412835.2:p.Thr703=
|
|
ENST00000635849.1:c.1272C>T
|
ENSP00000490948.1:p.Thr424=
|
|
ENST00000635957.1:c.906C>T
|
ENSP00000490385.1:p.Thr302=
|
|
ENST00000636930.2:c.3951C>T
MANE Select
|
ENSP00000490491.2:p.Thr1317=
|
|
ENST00000636940.1:n.1948C>T
|
|
|
ENST00000637015.1:c.1319C>T
|
|
|
ENST00000637568.1:c.1233C>T
|
|
|
ENST00000637741.1:n.617C>T
|
|
|
ENST00000637810.1:c.1293C>T
|
ENSP00000489636.1:p.Thr431=
|
|
ENST00000637904.1:c.1452C>T
|
ENSP00000490550.1:p.Thr484=
|
|
ENST00000647938.1:c.3582C>T
|
ENSP00000498155.1:p.Thr1194=
|
|
ENST00000346085.9:c.3582C>T
|
ENSP00000344546.4:p.Thr1194=
|
|
ENST00000350026.9:c.3543C>T
|
ENSP00000055163.7:p.Thr1181=
|
|
ENST00000414678.6:c.2109C>T
|
ENSP00000412835.2:p.Thr703=
|
|
NM_017519.2:c.3543C>T
|
NP_059989.2:p.Thr1181=
|
|
NM_020732.3:c.3582C>T
|
NP_065783.3:p.Thr1194=
|
|
XM_005267069.3:c.3702C>T
|
XP_005267126.2:p.Thr1234=
|
|
XM_011535984.1:c.2781C>T
|
XP_011534286.1:p.Thr927=
|
|
XM_011535985.1:c.2601C>T
|
XP_011534287.1:p.Thr867=
|
|
XM_011535986.1:c.2361C>T
|
XP_011534288.1:p.Thr787=
|
|
XM_011535987.1:c.1980C>T
|
XP_011534289.1:p.Thr660=
|
|
XM_011535988.1:c.843C>T
|
XP_011534290.1:p.Thr281=
|
|
NM_001346813.1:c.3702C>T
|
NP_001333742.1:p.Thr1234=
|
|
NM_001363725.1:c.1452C>T
|
NP_001350654.1:p.Thr484=
|
|
XM_011535984.2:c.3912C>T
|
XP_011534286.2:p.Thr1304=
|
|
XM_011535988.3:c.843C>T
|
XP_011534290.1:p.Thr281=
|
|
XM_017011103.2:c.3813C>T
|
XP_016866592.1:p.Thr1271=
|
|
XM_017011104.1:c.3783C>T
|
XP_016866593.1:p.Thr1261=
|
|
XM_017011105.2:c.3753C>T
|
XP_016866594.1:p.Thr1251=
|
|
XM_017011106.2:c.3624C>T
|
XP_016866595.1:p.Thr1208=
|
|
XM_017011107.2:c.3603C>T
|
XP_016866596.1:p.Thr1201=
|
|
XR_002956289.1:n.3995C>T
|
|
|
NM_001363725.2:c.1452C>T
|
NP_001350654.1:p.Thr484=
|
|
NM_001371656.1:c.3831C>T
|
NP_001358585.1:p.Thr1277=
|
|
NM_001374820.1:c.3831C>T
|
NP_001361749.1:p.Thr1277=
|
|
NM_001374828.1:c.3951C>T
MANE Select
|
NP_001361757.1:p.Thr1317=
|
|
NM_017519.3:c.3792C>T
|
NP_059989.3:p.Thr1264=
|
|