ENST00000350026.11:c.3914G>A
|
ENSP00000055163.8:p.Ser1305Asn
|
|
ENST00000414678.8:c.3983G>A
|
ENSP00000412835.3:p.Ser1328Asn
|
|
ENST00000637015.2:c.4202G>A
|
ENSP00000489729.2:p.Ser1401Asn
|
|
ENST00000346085.10:c.3953G>A
|
ENSP00000344546.5:p.Ser1318Asn
|
|
ENST00000350026.10:c.3665G>A
|
ENSP00000055163.7:p.Ser1222Asn
|
|
ENST00000414678.7:c.2231G>A
|
ENSP00000412835.2:p.Ser744Asn
|
|
ENST00000635849.1:c.1394G>A
|
ENSP00000490948.1:p.Ser465Asn
|
|
ENST00000635957.1:c.1025G>A
|
ENSP00000490385.1:p.Ser342Asn
|
|
ENST00000636930.2:c.4073G>A
MANE Select
|
ENSP00000490491.2:p.Ser1358Asn
|
|
ENST00000636940.1:n.2070G>A
|
|
|
ENST00000637015.1:c.1441G>A
|
|
|
ENST00000637568.1:c.1355G>A
|
|
|
ENST00000637741.1:n.739G>A
|
|
|
ENST00000637810.1:c.1415G>A
|
ENSP00000489636.1:p.Ser472Asn
|
|
ENST00000637904.1:c.1574G>A
|
ENSP00000490550.1:p.Ser525Asn
|
|
ENST00000647938.1:c.3704G>A
|
ENSP00000498155.1:p.Ser1235Asn
|
|
ENST00000346085.9:c.3704G>A
|
ENSP00000344546.4:p.Ser1235Asn
|
|
ENST00000350026.9:c.3665G>A
|
ENSP00000055163.7:p.Ser1222Asn
|
|
ENST00000414678.6:c.2231G>A
|
ENSP00000412835.2:p.Ser744Asn
|
|
NM_017519.2:c.3665G>A
|
NP_059989.2:p.Ser1222Asn
|
|
NM_020732.3:c.3704G>A
|
NP_065783.3:p.Ser1235Asn
|
|
XM_005267069.3:c.3824G>A
|
XP_005267126.2:p.Ser1275Asn
|
|
XM_011535984.1:c.2903G>A
|
XP_011534286.1:p.Ser968Asn
|
|
XM_011535985.1:c.2723G>A
|
XP_011534287.1:p.Ser908Asn
|
|
XM_011535986.1:c.2483G>A
|
XP_011534288.1:p.Ser828Asn
|
|
XM_011535987.1:c.2102G>A
|
XP_011534289.1:p.Ser701Asn
|
|
XM_011535988.1:c.965G>A
|
XP_011534290.1:p.Ser322Asn
|
|
NM_001346813.1:c.3824G>A
|
NP_001333742.1:p.Ser1275Asn
|
|
NM_001363725.1:c.1574G>A
|
NP_001350654.1:p.Ser525Asn
|
|
XM_011535984.2:c.4034G>A
|
XP_011534286.2:p.Ser1345Asn
|
|
XM_011535988.3:c.965G>A
|
XP_011534290.1:p.Ser322Asn
|
|
XM_017011103.2:c.3935G>A
|
XP_016866592.1:p.Ser1312Asn
|
|
XM_017011104.1:c.3905G>A
|
XP_016866593.1:p.Ser1302Asn
|
|
XM_017011105.2:c.3875G>A
|
XP_016866594.1:p.Ser1292Asn
|
|
XM_017011106.2:c.3746G>A
|
XP_016866595.1:p.Ser1249Asn
|
|
XM_017011107.2:c.3725G>A
|
XP_016866596.1:p.Ser1242Asn
|
|
XR_002956289.1:n.4117G>A
|
|
|
NM_001363725.2:c.1574G>A
|
NP_001350654.1:p.Ser525Asn
|
|
NM_001371656.1:c.3953G>A
|
NP_001358585.1:p.Ser1318Asn
|
|
NM_001374820.1:c.3953G>A
|
NP_001361749.1:p.Ser1318Asn
|
|
NM_001374828.1:c.4073G>A
MANE Select
|
NP_001361757.1:p.Ser1358Asn
|
|
NM_017519.3:c.3914G>A
|
NP_059989.3:p.Ser1305Asn
|
|