ENST00000350026.11:c.4980C>A
|
ENSP00000055163.8:p.Ser1660=
|
|
ENST00000414678.8:c.5049C>A
|
ENSP00000412835.3:p.Ser1683=
|
|
ENST00000637015.2:c.5268C>A
|
ENSP00000489729.2:p.Ser1756=
|
|
ENST00000346085.10:c.5019C>A
|
ENSP00000344546.5:p.Ser1673=
|
|
ENST00000350026.10:c.4731C>A
|
ENSP00000055163.7:p.Ser1577=
|
|
ENST00000414678.7:c.3297C>A
|
ENSP00000412835.2:p.Ser1099=
|
|
ENST00000635849.1:c.2460C>A
|
ENSP00000490948.1:p.Ser820=
|
|
ENST00000635957.1:c.2091C>A
|
ENSP00000490385.1:p.Ser697=
|
|
ENST00000636227.1:n.3602C>A
|
|
|
ENST00000636254.1:n.1059C>A
|
|
|
ENST00000636930.2:c.5139C>A
MANE Select
|
ENSP00000490491.2:p.Ser1713=
|
|
ENST00000636940.1:n.3136C>A
|
|
|
ENST00000637015.1:c.2507C>A
|
|
|
ENST00000637568.1:c.2421C>A
|
|
|
ENST00000637741.1:n.1805C>A
|
|
|
ENST00000637810.1:c.2481C>A
|
ENSP00000489636.1:p.Ser827=
|
|
ENST00000637904.1:c.2640C>A
|
ENSP00000490550.1:p.Ser880=
|
|
ENST00000647938.1:c.4770C>A
|
ENSP00000498155.1:p.Ser1590=
|
|
ENST00000346085.9:c.4770C>A
|
ENSP00000344546.4:p.Ser1590=
|
|
ENST00000350026.9:c.4731C>A
|
ENSP00000055163.7:p.Ser1577=
|
|
ENST00000414678.6:c.3297C>A
|
ENSP00000412835.2:p.Ser1099=
|
|
NM_017519.2:c.4731C>A
|
NP_059989.2:p.Ser1577=
|
|
NM_020732.3:c.4770C>A
|
NP_065783.3:p.Ser1590=
|
|
XM_005267069.3:c.4890C>A
|
XP_005267126.2:p.Ser1630=
|
|
XM_011535984.1:c.3969C>A
|
XP_011534286.1:p.Ser1323=
|
|
XM_011535985.1:c.3789C>A
|
XP_011534287.1:p.Ser1263=
|
|
XM_011535986.1:c.3549C>A
|
XP_011534288.1:p.Ser1183=
|
|
XM_011535987.1:c.3168C>A
|
XP_011534289.1:p.Ser1056=
|
|
XM_011535988.1:c.2031C>A
|
XP_011534290.1:p.Ser677=
|
|
NM_001346813.1:c.4890C>A
|
NP_001333742.1:p.Ser1630=
|
|
NM_001363725.1:c.2640C>A
|
NP_001350654.1:p.Ser880=
|
|
XM_011535984.2:c.5100C>A
|
XP_011534286.2:p.Ser1700=
|
|
XM_011535988.3:c.2031C>A
|
XP_011534290.1:p.Ser677=
|
|
XM_017011103.2:c.5001C>A
|
XP_016866592.1:p.Ser1667=
|
|
XM_017011104.1:c.4971C>A
|
XP_016866593.1:p.Ser1657=
|
|
XM_017011105.2:c.4941C>A
|
XP_016866594.1:p.Ser1647=
|
|
XM_017011106.2:c.4812C>A
|
XP_016866595.1:p.Ser1604=
|
|
XM_017011107.2:c.4791C>A
|
XP_016866596.1:p.Ser1597=
|
|
XR_002956289.1:n.5086C>A
|
|
|
NM_001363725.2:c.2640C>A
|
NP_001350654.1:p.Ser880=
|
|
NM_001371656.1:c.5019C>A
|
NP_001358585.1:p.Ser1673=
|
|
NM_001374820.1:c.5019C>A
|
NP_001361749.1:p.Ser1673=
|
|
NM_001374828.1:c.5139C>A
MANE Select
|
NP_001361757.1:p.Ser1713=
|
|
NM_017519.3:c.4980C>A
|
NP_059989.3:p.Ser1660=
|
|