ENST00000350026.11:c.4572G>A
|
ENSP00000055163.8:p.Ser1524=
|
|
ENST00000414678.8:c.4641G>A
|
ENSP00000412835.3:p.Ser1547=
|
|
ENST00000637015.2:c.4860G>A
|
ENSP00000489729.2:p.Ser1620=
|
|
ENST00000346085.10:c.4611G>A
|
ENSP00000344546.5:p.Ser1537=
|
|
ENST00000350026.10:c.4323G>A
|
ENSP00000055163.7:p.Ser1441=
|
|
ENST00000414678.7:c.2889G>A
|
ENSP00000412835.2:p.Ser963=
|
|
ENST00000635849.1:c.2052G>A
|
ENSP00000490948.1:p.Ser684=
|
|
ENST00000635957.1:c.1683G>A
|
ENSP00000490385.1:p.Ser561=
|
|
ENST00000636227.1:n.3194G>A
|
|
|
ENST00000636254.1:n.651G>A
|
|
|
ENST00000636930.2:c.4731G>A
MANE Select
|
ENSP00000490491.2:p.Ser1577=
|
|
ENST00000636940.1:n.2728G>A
|
|
|
ENST00000637015.1:c.2099G>A
|
|
|
ENST00000637568.1:c.2013G>A
|
|
|
ENST00000637741.1:n.1397G>A
|
|
|
ENST00000637810.1:c.2073G>A
|
ENSP00000489636.1:p.Ser691=
|
|
ENST00000637904.1:c.2232G>A
|
ENSP00000490550.1:p.Ser744=
|
|
ENST00000647938.1:c.4362G>A
|
ENSP00000498155.1:p.Ser1454=
|
|
ENST00000346085.9:c.4362G>A
|
ENSP00000344546.4:p.Ser1454=
|
|
ENST00000350026.9:c.4323G>A
|
ENSP00000055163.7:p.Ser1441=
|
|
ENST00000414678.6:c.2889G>A
|
ENSP00000412835.2:p.Ser963=
|
|
NM_017519.2:c.4323G>A
|
NP_059989.2:p.Ser1441=
|
|
NM_020732.3:c.4362G>A
|
NP_065783.3:p.Ser1454=
|
|
XM_005267069.3:c.4482G>A
|
XP_005267126.2:p.Ser1494=
|
|
XM_011535984.1:c.3561G>A
|
XP_011534286.1:p.Ser1187=
|
|
XM_011535985.1:c.3381G>A
|
XP_011534287.1:p.Ser1127=
|
|
XM_011535986.1:c.3141G>A
|
XP_011534288.1:p.Ser1047=
|
|
XM_011535987.1:c.2760G>A
|
XP_011534289.1:p.Ser920=
|
|
XM_011535988.1:c.1623G>A
|
XP_011534290.1:p.Ser541=
|
|
NM_001346813.1:c.4482G>A
|
NP_001333742.1:p.Ser1494=
|
|
NM_001363725.1:c.2232G>A
|
NP_001350654.1:p.Ser744=
|
|
XM_011535984.2:c.4692G>A
|
XP_011534286.2:p.Ser1564=
|
|
XM_011535988.3:c.1623G>A
|
XP_011534290.1:p.Ser541=
|
|
XM_017011103.2:c.4593G>A
|
XP_016866592.1:p.Ser1531=
|
|
XM_017011104.1:c.4563G>A
|
XP_016866593.1:p.Ser1521=
|
|
XM_017011105.2:c.4533G>A
|
XP_016866594.1:p.Ser1511=
|
|
XM_017011106.2:c.4404G>A
|
XP_016866595.1:p.Ser1468=
|
|
XM_017011107.2:c.4383G>A
|
XP_016866596.1:p.Ser1461=
|
|
XR_002956289.1:n.4678G>A
|
|
|
NM_001363725.2:c.2232G>A
|
NP_001350654.1:p.Ser744=
|
|
NM_001371656.1:c.4611G>A
|
NP_001358585.1:p.Ser1537=
|
|
NM_001374820.1:c.4611G>A
|
NP_001361749.1:p.Ser1537=
|
|
NM_001374828.1:c.4731G>A
MANE Select
|
NP_001361757.1:p.Ser1577=
|
|
NM_017519.3:c.4572G>A
|
NP_059989.3:p.Ser1524=
|
|