ENST00000350026.11:c.4919G>C
|
ENSP00000055163.8:p.Ser1640Thr
|
|
ENST00000414678.8:c.4988G>C
|
ENSP00000412835.3:p.Ser1663Thr
|
|
ENST00000637015.2:c.5207G>C
|
ENSP00000489729.2:p.Ser1736Thr
|
|
ENST00000346085.10:c.4958G>C
|
ENSP00000344546.5:p.Ser1653Thr
|
|
ENST00000350026.10:c.4670G>C
|
ENSP00000055163.7:p.Ser1557Thr
|
|
ENST00000414678.7:c.3236G>C
|
ENSP00000412835.2:p.Ser1079Thr
|
|
ENST00000635849.1:c.2399G>C
|
ENSP00000490948.1:p.Ser800Thr
|
|
ENST00000635957.1:c.2030G>C
|
ENSP00000490385.1:p.Ser677Thr
|
|
ENST00000636227.1:n.3541G>C
|
|
|
ENST00000636254.1:n.998G>C
|
|
|
ENST00000636930.2:c.5078G>C
MANE Select
|
ENSP00000490491.2:p.Ser1693Thr
|
|
ENST00000636940.1:n.3075G>C
|
|
|
ENST00000637015.1:c.2446G>C
|
|
|
ENST00000637568.1:c.2360G>C
|
|
|
ENST00000637741.1:n.1744G>C
|
|
|
ENST00000637810.1:c.2420G>C
|
ENSP00000489636.1:p.Ser807Thr
|
|
ENST00000637904.1:c.2579G>C
|
ENSP00000490550.1:p.Ser860Thr
|
|
ENST00000647938.1:c.4709G>C
|
ENSP00000498155.1:p.Ser1570Thr
|
|
ENST00000346085.9:c.4709G>C
|
ENSP00000344546.4:p.Ser1570Thr
|
|
ENST00000350026.9:c.4670G>C
|
ENSP00000055163.7:p.Ser1557Thr
|
|
ENST00000414678.6:c.3236G>C
|
ENSP00000412835.2:p.Ser1079Thr
|
|
NM_017519.2:c.4670G>C
|
NP_059989.2:p.Ser1557Thr
|
|
NM_020732.3:c.4709G>C
|
NP_065783.3:p.Ser1570Thr
|
|
XM_005267069.3:c.4829G>C
|
XP_005267126.2:p.Ser1610Thr
|
|
XM_011535984.1:c.3908G>C
|
XP_011534286.1:p.Ser1303Thr
|
|
XM_011535985.1:c.3728G>C
|
XP_011534287.1:p.Ser1243Thr
|
|
XM_011535986.1:c.3488G>C
|
XP_011534288.1:p.Ser1163Thr
|
|
XM_011535987.1:c.3107G>C
|
XP_011534289.1:p.Ser1036Thr
|
|
XM_011535988.1:c.1970G>C
|
XP_011534290.1:p.Ser657Thr
|
|
NM_001346813.1:c.4829G>C
|
NP_001333742.1:p.Ser1610Thr
|
|
NM_001363725.1:c.2579G>C
|
NP_001350654.1:p.Ser860Thr
|
|
XM_011535984.2:c.5039G>C
|
XP_011534286.2:p.Ser1680Thr
|
|
XM_011535988.3:c.1970G>C
|
XP_011534290.1:p.Ser657Thr
|
|
XM_017011103.2:c.4940G>C
|
XP_016866592.1:p.Ser1647Thr
|
|
XM_017011104.1:c.4910G>C
|
XP_016866593.1:p.Ser1637Thr
|
|
XM_017011105.2:c.4880G>C
|
XP_016866594.1:p.Ser1627Thr
|
|
XM_017011106.2:c.4751G>C
|
XP_016866595.1:p.Ser1584Thr
|
|
XM_017011107.2:c.4730G>C
|
XP_016866596.1:p.Ser1577Thr
|
|
XR_002956289.1:n.5025G>C
|
|
|
NM_001363725.2:c.2579G>C
|
NP_001350654.1:p.Ser860Thr
|
|
NM_001371656.1:c.4958G>C
|
NP_001358585.1:p.Ser1653Thr
|
|
NM_001374820.1:c.4958G>C
|
NP_001361749.1:p.Ser1653Thr
|
|
NM_001374828.1:c.5078G>C
MANE Select
|
NP_001361757.1:p.Ser1693Thr
|
|
NM_017519.3:c.4919G>C
|
NP_059989.3:p.Ser1640Thr
|
|