ENST00000350026.11:c.4926T>C
|
ENSP00000055163.8:p.Ser1642=
|
|
ENST00000414678.8:c.4995T>C
|
ENSP00000412835.3:p.Ser1665=
|
|
ENST00000637015.2:c.5214T>C
|
ENSP00000489729.2:p.Ser1738=
|
|
ENST00000346085.10:c.4965T>C
|
ENSP00000344546.5:p.Ser1655=
|
|
ENST00000350026.10:c.4677T>C
|
ENSP00000055163.7:p.Ser1559=
|
|
ENST00000414678.7:c.3243T>C
|
ENSP00000412835.2:p.Ser1081=
|
|
ENST00000635849.1:c.2406T>C
|
ENSP00000490948.1:p.Ser802=
|
|
ENST00000635957.1:c.2037T>C
|
ENSP00000490385.1:p.Ser679=
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|
ENST00000636227.1:n.3548T>C
|
|
|
ENST00000636254.1:n.1005T>C
|
|
|
ENST00000636930.2:c.5085T>C
MANE Select
|
ENSP00000490491.2:p.Ser1695=
|
|
ENST00000636940.1:n.3082T>C
|
|
|
ENST00000637015.1:c.2453T>C
|
|
|
ENST00000637568.1:c.2367T>C
|
|
|
ENST00000637741.1:n.1751T>C
|
|
|
ENST00000637810.1:c.2427T>C
|
ENSP00000489636.1:p.Ser809=
|
|
ENST00000637904.1:c.2586T>C
|
ENSP00000490550.1:p.Ser862=
|
|
ENST00000647938.1:c.4716T>C
|
ENSP00000498155.1:p.Ser1572=
|
|
ENST00000346085.9:c.4716T>C
|
ENSP00000344546.4:p.Ser1572=
|
|
ENST00000350026.9:c.4677T>C
|
ENSP00000055163.7:p.Ser1559=
|
|
ENST00000414678.6:c.3243T>C
|
ENSP00000412835.2:p.Ser1081=
|
|
NM_017519.2:c.4677T>C
|
NP_059989.2:p.Ser1559=
|
|
NM_020732.3:c.4716T>C
|
NP_065783.3:p.Ser1572=
|
|
XM_005267069.3:c.4836T>C
|
XP_005267126.2:p.Ser1612=
|
|
XM_011535984.1:c.3915T>C
|
XP_011534286.1:p.Ser1305=
|
|
XM_011535985.1:c.3735T>C
|
XP_011534287.1:p.Ser1245=
|
|
XM_011535986.1:c.3495T>C
|
XP_011534288.1:p.Ser1165=
|
|
XM_011535987.1:c.3114T>C
|
XP_011534289.1:p.Ser1038=
|
|
XM_011535988.1:c.1977T>C
|
XP_011534290.1:p.Ser659=
|
|
NM_001346813.1:c.4836T>C
|
NP_001333742.1:p.Ser1612=
|
|
NM_001363725.1:c.2586T>C
|
NP_001350654.1:p.Ser862=
|
|
XM_011535984.2:c.5046T>C
|
XP_011534286.2:p.Ser1682=
|
|
XM_011535988.3:c.1977T>C
|
XP_011534290.1:p.Ser659=
|
|
XM_017011103.2:c.4947T>C
|
XP_016866592.1:p.Ser1649=
|
|
XM_017011104.1:c.4917T>C
|
XP_016866593.1:p.Ser1639=
|
|
XM_017011105.2:c.4887T>C
|
XP_016866594.1:p.Ser1629=
|
|
XM_017011106.2:c.4758T>C
|
XP_016866595.1:p.Ser1586=
|
|
XM_017011107.2:c.4737T>C
|
XP_016866596.1:p.Ser1579=
|
|
XR_002956289.1:n.5032T>C
|
|
|
NM_001363725.2:c.2586T>C
|
NP_001350654.1:p.Ser862=
|
|
NM_001371656.1:c.4965T>C
|
NP_001358585.1:p.Ser1655=
|
|
NM_001374820.1:c.4965T>C
|
NP_001361749.1:p.Ser1655=
|
|
NM_001374828.1:c.5085T>C
MANE Select
|
NP_001361757.1:p.Ser1695=
|
|
NM_017519.3:c.4926T>C
|
NP_059989.3:p.Ser1642=
|
|