ENST00000350026.11:c.3909A>C
|
ENSP00000055163.8:p.Thr1303=
|
|
ENST00000414678.8:c.3978A>C
|
ENSP00000412835.3:p.Thr1326=
|
|
ENST00000637015.2:c.4197A>C
|
ENSP00000489729.2:p.Thr1399=
|
|
ENST00000346085.10:c.3948A>C
|
ENSP00000344546.5:p.Thr1316=
|
|
ENST00000350026.10:c.3660A>C
|
ENSP00000055163.7:p.Thr1220=
|
|
ENST00000414678.7:c.2226A>C
|
ENSP00000412835.2:p.Thr742=
|
|
ENST00000635849.1:c.1389A>C
|
ENSP00000490948.1:p.Thr463=
|
|
ENST00000635957.1:c.1020A>C
|
ENSP00000490385.1:p.Thr340=
|
|
ENST00000636930.2:c.4068A>C
MANE Select
|
ENSP00000490491.2:p.Thr1356=
|
|
ENST00000636940.1:n.2065A>C
|
|
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ENST00000637015.1:c.1436A>C
|
|
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ENST00000637568.1:c.1350A>C
|
|
|
ENST00000637741.1:n.734A>C
|
|
|
ENST00000637810.1:c.1410A>C
|
ENSP00000489636.1:p.Thr470=
|
|
ENST00000637904.1:c.1569A>C
|
ENSP00000490550.1:p.Thr523=
|
|
ENST00000647938.1:c.3699A>C
|
ENSP00000498155.1:p.Thr1233=
|
|
ENST00000346085.9:c.3699A>C
|
ENSP00000344546.4:p.Thr1233=
|
|
ENST00000350026.9:c.3660A>C
|
ENSP00000055163.7:p.Thr1220=
|
|
ENST00000414678.6:c.2226A>C
|
ENSP00000412835.2:p.Thr742=
|
|
NM_017519.2:c.3660A>C
|
NP_059989.2:p.Thr1220=
|
|
NM_020732.3:c.3699A>C
|
NP_065783.3:p.Thr1233=
|
|
XM_005267069.3:c.3819A>C
|
XP_005267126.2:p.Thr1273=
|
|
XM_011535984.1:c.2898A>C
|
XP_011534286.1:p.Thr966=
|
|
XM_011535985.1:c.2718A>C
|
XP_011534287.1:p.Thr906=
|
|
XM_011535986.1:c.2478A>C
|
XP_011534288.1:p.Thr826=
|
|
XM_011535987.1:c.2097A>C
|
XP_011534289.1:p.Thr699=
|
|
XM_011535988.1:c.960A>C
|
XP_011534290.1:p.Thr320=
|
|
NM_001346813.1:c.3819A>C
|
NP_001333742.1:p.Thr1273=
|
|
NM_001363725.1:c.1569A>C
|
NP_001350654.1:p.Thr523=
|
|
XM_011535984.2:c.4029A>C
|
XP_011534286.2:p.Thr1343=
|
|
XM_011535988.3:c.960A>C
|
XP_011534290.1:p.Thr320=
|
|
XM_017011103.2:c.3930A>C
|
XP_016866592.1:p.Thr1310=
|
|
XM_017011104.1:c.3900A>C
|
XP_016866593.1:p.Thr1300=
|
|
XM_017011105.2:c.3870A>C
|
XP_016866594.1:p.Thr1290=
|
|
XM_017011106.2:c.3741A>C
|
XP_016866595.1:p.Thr1247=
|
|
XM_017011107.2:c.3720A>C
|
XP_016866596.1:p.Thr1240=
|
|
XR_002956289.1:n.4112A>C
|
|
|
NM_001363725.2:c.1569A>C
|
NP_001350654.1:p.Thr523=
|
|
NM_001371656.1:c.3948A>C
|
NP_001358585.1:p.Thr1316=
|
|
NM_001374820.1:c.3948A>C
|
NP_001361749.1:p.Thr1316=
|
|
NM_001374828.1:c.4068A>C
MANE Select
|
NP_001361757.1:p.Thr1356=
|
|
NM_017519.3:c.3909A>C
|
NP_059989.3:p.Thr1303=
|
|