ENST00000350026.11:c.3850A>T
|
ENSP00000055163.8:p.Thr1284Ser
|
|
ENST00000414678.8:c.3919A>T
|
ENSP00000412835.3:p.Thr1307Ser
|
|
ENST00000637015.2:c.4138A>T
|
ENSP00000489729.2:p.Thr1380Ser
|
|
ENST00000346085.10:c.3889A>T
|
ENSP00000344546.5:p.Thr1297Ser
|
|
ENST00000350026.10:c.3601A>T
|
ENSP00000055163.7:p.Thr1201Ser
|
|
ENST00000414678.7:c.2167A>T
|
ENSP00000412835.2:p.Thr723Ser
|
|
ENST00000635849.1:c.1330A>T
|
ENSP00000490948.1:p.Thr444Ser
|
|
ENST00000635957.1:c.964A>T
|
ENSP00000490385.1:p.Thr322Ser
|
|
ENST00000636930.2:c.4009A>T
MANE Select
|
ENSP00000490491.2:p.Thr1337Ser
|
|
ENST00000636940.1:n.2006A>T
|
|
|
ENST00000637015.1:c.1377A>T
|
|
|
ENST00000637568.1:c.1291A>T
|
|
|
ENST00000637741.1:n.675A>T
|
|
|
ENST00000637810.1:c.1351A>T
|
ENSP00000489636.1:p.Thr451Ser
|
|
ENST00000637904.1:c.1510A>T
|
ENSP00000490550.1:p.Thr504Ser
|
|
ENST00000647938.1:c.3640A>T
|
ENSP00000498155.1:p.Thr1214Ser
|
|
ENST00000346085.9:c.3640A>T
|
ENSP00000344546.4:p.Thr1214Ser
|
|
ENST00000350026.9:c.3601A>T
|
ENSP00000055163.7:p.Thr1201Ser
|
|
ENST00000414678.6:c.2167A>T
|
ENSP00000412835.2:p.Thr723Ser
|
|
NM_017519.2:c.3601A>T
|
NP_059989.2:p.Thr1201Ser
|
|
NM_020732.3:c.3640A>T
|
NP_065783.3:p.Thr1214Ser
|
|
XM_005267069.3:c.3760A>T
|
XP_005267126.2:p.Thr1254Ser
|
|
XM_011535984.1:c.2839A>T
|
XP_011534286.1:p.Thr947Ser
|
|
XM_011535985.1:c.2659A>T
|
XP_011534287.1:p.Thr887Ser
|
|
XM_011535986.1:c.2419A>T
|
XP_011534288.1:p.Thr807Ser
|
|
XM_011535987.1:c.2038A>T
|
XP_011534289.1:p.Thr680Ser
|
|
XM_011535988.1:c.901A>T
|
XP_011534290.1:p.Thr301Ser
|
|
NM_001346813.1:c.3760A>T
|
NP_001333742.1:p.Thr1254Ser
|
|
NM_001363725.1:c.1510A>T
|
NP_001350654.1:p.Thr504Ser
|
|
XM_011535984.2:c.3970A>T
|
XP_011534286.2:p.Thr1324Ser
|
|
XM_011535988.3:c.901A>T
|
XP_011534290.1:p.Thr301Ser
|
|
XM_017011103.2:c.3871A>T
|
XP_016866592.1:p.Thr1291Ser
|
|
XM_017011104.1:c.3841A>T
|
XP_016866593.1:p.Thr1281Ser
|
|
XM_017011105.2:c.3811A>T
|
XP_016866594.1:p.Thr1271Ser
|
|
XM_017011106.2:c.3682A>T
|
XP_016866595.1:p.Thr1228Ser
|
|
XM_017011107.2:c.3661A>T
|
XP_016866596.1:p.Thr1221Ser
|
|
XR_002956289.1:n.4053A>T
|
|
|
NM_001363725.2:c.1510A>T
|
NP_001350654.1:p.Thr504Ser
|
|
NM_001371656.1:c.3889A>T
|
NP_001358585.1:p.Thr1297Ser
|
|
NM_001374820.1:c.3889A>T
|
NP_001361749.1:p.Thr1297Ser
|
|
NM_001374828.1:c.4009A>T
MANE Select
|
NP_001361757.1:p.Thr1337Ser
|
|
NM_017519.3:c.3850A>T
|
NP_059989.3:p.Thr1284Ser
|
|