ENST00000350026.11:c.3791C>A
|
ENSP00000055163.8:p.Thr1264Asn
|
|
ENST00000414678.8:c.3860C>A
|
ENSP00000412835.3:p.Thr1287Asn
|
|
ENST00000637015.2:c.4079C>A
|
ENSP00000489729.2:p.Thr1360Asn
|
|
ENST00000346085.10:c.3830C>A
|
ENSP00000344546.5:p.Thr1277Asn
|
|
ENST00000350026.10:c.3542C>A
|
ENSP00000055163.7:p.Thr1181Asn
|
|
ENST00000414678.7:c.2108C>A
|
ENSP00000412835.2:p.Thr703Asn
|
|
ENST00000635849.1:c.1271C>A
|
ENSP00000490948.1:p.Thr424Asn
|
|
ENST00000635957.1:c.905C>A
|
ENSP00000490385.1:p.Thr302Asn
|
|
ENST00000636930.2:c.3950C>A
MANE Select
|
ENSP00000490491.2:p.Thr1317Asn
|
|
ENST00000636940.1:n.1947C>A
|
|
|
ENST00000637015.1:c.1318C>A
|
|
|
ENST00000637568.1:c.1232C>A
|
|
|
ENST00000637741.1:n.616C>A
|
|
|
ENST00000637810.1:c.1292C>A
|
ENSP00000489636.1:p.Thr431Asn
|
|
ENST00000637904.1:c.1451C>A
|
ENSP00000490550.1:p.Thr484Asn
|
|
ENST00000647938.1:c.3581C>A
|
ENSP00000498155.1:p.Thr1194Asn
|
|
ENST00000346085.9:c.3581C>A
|
ENSP00000344546.4:p.Thr1194Asn
|
|
ENST00000350026.9:c.3542C>A
|
ENSP00000055163.7:p.Thr1181Asn
|
|
ENST00000414678.6:c.2108C>A
|
ENSP00000412835.2:p.Thr703Asn
|
|
NM_017519.2:c.3542C>A
|
NP_059989.2:p.Thr1181Asn
|
|
NM_020732.3:c.3581C>A
|
NP_065783.3:p.Thr1194Asn
|
|
XM_005267069.3:c.3701C>A
|
XP_005267126.2:p.Thr1234Asn
|
|
XM_011535984.1:c.2780C>A
|
XP_011534286.1:p.Thr927Asn
|
|
XM_011535985.1:c.2600C>A
|
XP_011534287.1:p.Thr867Asn
|
|
XM_011535986.1:c.2360C>A
|
XP_011534288.1:p.Thr787Asn
|
|
XM_011535987.1:c.1979C>A
|
XP_011534289.1:p.Thr660Asn
|
|
XM_011535988.1:c.842C>A
|
XP_011534290.1:p.Thr281Asn
|
|
NM_001346813.1:c.3701C>A
|
NP_001333742.1:p.Thr1234Asn
|
|
NM_001363725.1:c.1451C>A
|
NP_001350654.1:p.Thr484Asn
|
|
XM_011535984.2:c.3911C>A
|
XP_011534286.2:p.Thr1304Asn
|
|
XM_011535988.3:c.842C>A
|
XP_011534290.1:p.Thr281Asn
|
|
XM_017011103.2:c.3812C>A
|
XP_016866592.1:p.Thr1271Asn
|
|
XM_017011104.1:c.3782C>A
|
XP_016866593.1:p.Thr1261Asn
|
|
XM_017011105.2:c.3752C>A
|
XP_016866594.1:p.Thr1251Asn
|
|
XM_017011106.2:c.3623C>A
|
XP_016866595.1:p.Thr1208Asn
|
|
XM_017011107.2:c.3602C>A
|
XP_016866596.1:p.Thr1201Asn
|
|
XR_002956289.1:n.3994C>A
|
|
|
NM_001363725.2:c.1451C>A
|
NP_001350654.1:p.Thr484Asn
|
|
NM_001371656.1:c.3830C>A
|
NP_001358585.1:p.Thr1277Asn
|
|
NM_001374820.1:c.3830C>A
|
NP_001361749.1:p.Thr1277Asn
|
|
NM_001374828.1:c.3950C>A
MANE Select
|
NP_001361757.1:p.Thr1317Asn
|
|
NM_017519.3:c.3791C>A
|
NP_059989.3:p.Thr1264Asn
|
|