ENST00000350026.11:c.4894T>A
|
ENSP00000055163.8:p.Ser1632Thr
|
|
ENST00000414678.8:c.4963T>A
|
ENSP00000412835.3:p.Ser1655Thr
|
|
ENST00000637015.2:c.5182T>A
|
ENSP00000489729.2:p.Ser1728Thr
|
|
ENST00000346085.10:c.4933T>A
|
ENSP00000344546.5:p.Ser1645Thr
|
|
ENST00000350026.10:c.4645T>A
|
ENSP00000055163.7:p.Ser1549Thr
|
|
ENST00000414678.7:c.3211T>A
|
ENSP00000412835.2:p.Ser1071Thr
|
|
ENST00000635849.1:c.2374T>A
|
ENSP00000490948.1:p.Ser792Thr
|
|
ENST00000635957.1:c.2005T>A
|
ENSP00000490385.1:p.Ser669Thr
|
|
ENST00000636227.1:n.3516T>A
|
|
|
ENST00000636254.1:n.973T>A
|
|
|
ENST00000636930.2:c.5053T>A
MANE Select
|
ENSP00000490491.2:p.Ser1685Thr
|
|
ENST00000636940.1:n.3050T>A
|
|
|
ENST00000637015.1:c.2421T>A
|
|
|
ENST00000637568.1:c.2335T>A
|
|
|
ENST00000637741.1:n.1719T>A
|
|
|
ENST00000637810.1:c.2395T>A
|
ENSP00000489636.1:p.Ser799Thr
|
|
ENST00000637904.1:c.2554T>A
|
ENSP00000490550.1:p.Ser852Thr
|
|
ENST00000647938.1:c.4684T>A
|
ENSP00000498155.1:p.Ser1562Thr
|
|
ENST00000346085.9:c.4684T>A
|
ENSP00000344546.4:p.Ser1562Thr
|
|
ENST00000350026.9:c.4645T>A
|
ENSP00000055163.7:p.Ser1549Thr
|
|
ENST00000414678.6:c.3211T>A
|
ENSP00000412835.2:p.Ser1071Thr
|
|
NM_017519.2:c.4645T>A
|
NP_059989.2:p.Ser1549Thr
|
|
NM_020732.3:c.4684T>A
|
NP_065783.3:p.Ser1562Thr
|
|
XM_005267069.3:c.4804T>A
|
XP_005267126.2:p.Ser1602Thr
|
|
XM_011535984.1:c.3883T>A
|
XP_011534286.1:p.Ser1295Thr
|
|
XM_011535985.1:c.3703T>A
|
XP_011534287.1:p.Ser1235Thr
|
|
XM_011535986.1:c.3463T>A
|
XP_011534288.1:p.Ser1155Thr
|
|
XM_011535987.1:c.3082T>A
|
XP_011534289.1:p.Ser1028Thr
|
|
XM_011535988.1:c.1945T>A
|
XP_011534290.1:p.Ser649Thr
|
|
NM_001346813.1:c.4804T>A
|
NP_001333742.1:p.Ser1602Thr
|
|
NM_001363725.1:c.2554T>A
|
NP_001350654.1:p.Ser852Thr
|
|
XM_011535984.2:c.5014T>A
|
XP_011534286.2:p.Ser1672Thr
|
|
XM_011535988.3:c.1945T>A
|
XP_011534290.1:p.Ser649Thr
|
|
XM_017011103.2:c.4915T>A
|
XP_016866592.1:p.Ser1639Thr
|
|
XM_017011104.1:c.4885T>A
|
XP_016866593.1:p.Ser1629Thr
|
|
XM_017011105.2:c.4855T>A
|
XP_016866594.1:p.Ser1619Thr
|
|
XM_017011106.2:c.4726T>A
|
XP_016866595.1:p.Ser1576Thr
|
|
XM_017011107.2:c.4705T>A
|
XP_016866596.1:p.Ser1569Thr
|
|
XR_002956289.1:n.5000T>A
|
|
|
NM_001363725.2:c.2554T>A
|
NP_001350654.1:p.Ser852Thr
|
|
NM_001371656.1:c.4933T>A
|
NP_001358585.1:p.Ser1645Thr
|
|
NM_001374820.1:c.4933T>A
|
NP_001361749.1:p.Ser1645Thr
|
|
NM_001374828.1:c.5053T>A
MANE Select
|
NP_001361757.1:p.Ser1685Thr
|
|
NM_017519.3:c.4894T>A
|
NP_059989.3:p.Ser1632Thr
|
|