ENST00000350026.11:c.4665A>G
|
ENSP00000055163.8:p.Thr1555=
|
|
ENST00000414678.8:c.4734A>G
|
ENSP00000412835.3:p.Thr1578=
|
|
ENST00000637015.2:c.4953A>G
|
ENSP00000489729.2:p.Thr1651=
|
|
ENST00000346085.10:c.4704A>G
|
ENSP00000344546.5:p.Thr1568=
|
|
ENST00000350026.10:c.4416A>G
|
ENSP00000055163.7:p.Thr1472=
|
|
ENST00000414678.7:c.2982A>G
|
ENSP00000412835.2:p.Thr994=
|
|
ENST00000635849.1:c.2145A>G
|
ENSP00000490948.1:p.Thr715=
|
|
ENST00000635957.1:c.1776A>G
|
ENSP00000490385.1:p.Thr592=
|
|
ENST00000636227.1:n.3287A>G
|
|
|
ENST00000636254.1:n.744A>G
|
|
|
ENST00000636930.2:c.4824A>G
MANE Select
|
ENSP00000490491.2:p.Thr1608=
|
|
ENST00000636940.1:n.2821A>G
|
|
|
ENST00000637015.1:c.2192A>G
|
|
|
ENST00000637568.1:c.2106A>G
|
|
|
ENST00000637741.1:n.1490A>G
|
|
|
ENST00000637810.1:c.2166A>G
|
ENSP00000489636.1:p.Thr722=
|
|
ENST00000637904.1:c.2325A>G
|
ENSP00000490550.1:p.Thr775=
|
|
ENST00000647938.1:c.4455A>G
|
ENSP00000498155.1:p.Thr1485=
|
|
ENST00000346085.9:c.4455A>G
|
ENSP00000344546.4:p.Thr1485=
|
|
ENST00000350026.9:c.4416A>G
|
ENSP00000055163.7:p.Thr1472=
|
|
ENST00000414678.6:c.2982A>G
|
ENSP00000412835.2:p.Thr994=
|
|
NM_017519.2:c.4416A>G
|
NP_059989.2:p.Thr1472=
|
|
NM_020732.3:c.4455A>G
|
NP_065783.3:p.Thr1485=
|
|
XM_005267069.3:c.4575A>G
|
XP_005267126.2:p.Thr1525=
|
|
XM_011535984.1:c.3654A>G
|
XP_011534286.1:p.Thr1218=
|
|
XM_011535985.1:c.3474A>G
|
XP_011534287.1:p.Thr1158=
|
|
XM_011535986.1:c.3234A>G
|
XP_011534288.1:p.Thr1078=
|
|
XM_011535987.1:c.2853A>G
|
XP_011534289.1:p.Thr951=
|
|
XM_011535988.1:c.1716A>G
|
XP_011534290.1:p.Thr572=
|
|
NM_001346813.1:c.4575A>G
|
NP_001333742.1:p.Thr1525=
|
|
NM_001363725.1:c.2325A>G
|
NP_001350654.1:p.Thr775=
|
|
XM_011535984.2:c.4785A>G
|
XP_011534286.2:p.Thr1595=
|
|
XM_011535988.3:c.1716A>G
|
XP_011534290.1:p.Thr572=
|
|
XM_017011103.2:c.4686A>G
|
XP_016866592.1:p.Thr1562=
|
|
XM_017011104.1:c.4656A>G
|
XP_016866593.1:p.Thr1552=
|
|
XM_017011105.2:c.4626A>G
|
XP_016866594.1:p.Thr1542=
|
|
XM_017011106.2:c.4497A>G
|
XP_016866595.1:p.Thr1499=
|
|
XM_017011107.2:c.4476A>G
|
XP_016866596.1:p.Thr1492=
|
|
XR_002956289.1:n.4771A>G
|
|
|
NM_001363725.2:c.2325A>G
|
NP_001350654.1:p.Thr775=
|
|
NM_001371656.1:c.4704A>G
|
NP_001358585.1:p.Thr1568=
|
|
NM_001374820.1:c.4704A>G
|
NP_001361749.1:p.Thr1568=
|
|
NM_001374828.1:c.4824A>G
MANE Select
|
NP_001361757.1:p.Thr1608=
|
|
NM_017519.3:c.4665A>G
|
NP_059989.3:p.Thr1555=
|
|