ENST00000350026.11:c.3905G>A
|
ENSP00000055163.8:p.Ser1302Asn
|
|
ENST00000414678.8:c.3974G>A
|
ENSP00000412835.3:p.Ser1325Asn
|
|
ENST00000637015.2:c.4193G>A
|
ENSP00000489729.2:p.Ser1398Asn
|
|
ENST00000346085.10:c.3944G>A
|
ENSP00000344546.5:p.Ser1315Asn
|
|
ENST00000350026.10:c.3656G>A
|
ENSP00000055163.7:p.Ser1219Asn
|
|
ENST00000414678.7:c.2222G>A
|
ENSP00000412835.2:p.Ser741Asn
|
|
ENST00000635849.1:c.1385G>A
|
ENSP00000490948.1:p.Ser462Asn
|
|
ENST00000635957.1:c.1016G>A
|
ENSP00000490385.1:p.Ser339Asn
|
|
ENST00000636930.2:c.4064G>A
MANE Select
|
ENSP00000490491.2:p.Ser1355Asn
|
|
ENST00000636940.1:n.2061G>A
|
|
|
ENST00000637015.1:c.1432G>A
|
|
|
ENST00000637568.1:c.1346G>A
|
|
|
ENST00000637741.1:n.730G>A
|
|
|
ENST00000637810.1:c.1406G>A
|
ENSP00000489636.1:p.Ser469Asn
|
|
ENST00000637904.1:c.1565G>A
|
ENSP00000490550.1:p.Ser522Asn
|
|
ENST00000647938.1:c.3695G>A
|
ENSP00000498155.1:p.Ser1232Asn
|
|
ENST00000346085.9:c.3695G>A
|
ENSP00000344546.4:p.Ser1232Asn
|
|
ENST00000350026.9:c.3656G>A
|
ENSP00000055163.7:p.Ser1219Asn
|
|
ENST00000414678.6:c.2222G>A
|
ENSP00000412835.2:p.Ser741Asn
|
|
NM_017519.2:c.3656G>A
|
NP_059989.2:p.Ser1219Asn
|
|
NM_020732.3:c.3695G>A
|
NP_065783.3:p.Ser1232Asn
|
|
XM_005267069.3:c.3815G>A
|
XP_005267126.2:p.Ser1272Asn
|
|
XM_011535984.1:c.2894G>A
|
XP_011534286.1:p.Ser965Asn
|
|
XM_011535985.1:c.2714G>A
|
XP_011534287.1:p.Ser905Asn
|
|
XM_011535986.1:c.2474G>A
|
XP_011534288.1:p.Ser825Asn
|
|
XM_011535987.1:c.2093G>A
|
XP_011534289.1:p.Ser698Asn
|
|
XM_011535988.1:c.956G>A
|
XP_011534290.1:p.Ser319Asn
|
|
NM_001346813.1:c.3815G>A
|
NP_001333742.1:p.Ser1272Asn
|
|
NM_001363725.1:c.1565G>A
|
NP_001350654.1:p.Ser522Asn
|
|
XM_011535984.2:c.4025G>A
|
XP_011534286.2:p.Ser1342Asn
|
|
XM_011535988.3:c.956G>A
|
XP_011534290.1:p.Ser319Asn
|
|
XM_017011103.2:c.3926G>A
|
XP_016866592.1:p.Ser1309Asn
|
|
XM_017011104.1:c.3896G>A
|
XP_016866593.1:p.Ser1299Asn
|
|
XM_017011105.2:c.3866G>A
|
XP_016866594.1:p.Ser1289Asn
|
|
XM_017011106.2:c.3737G>A
|
XP_016866595.1:p.Ser1246Asn
|
|
XM_017011107.2:c.3716G>A
|
XP_016866596.1:p.Ser1239Asn
|
|
XR_002956289.1:n.4108G>A
|
|
|
NM_001363725.2:c.1565G>A
|
NP_001350654.1:p.Ser522Asn
|
|
NM_001371656.1:c.3944G>A
|
NP_001358585.1:p.Ser1315Asn
|
|
NM_001374820.1:c.3944G>A
|
NP_001361749.1:p.Ser1315Asn
|
|
NM_001374828.1:c.4064G>A
MANE Select
|
NP_001361757.1:p.Ser1355Asn
|
|
NM_017519.3:c.3905G>A
|
NP_059989.3:p.Ser1302Asn
|
|