ENST00000350026.11:c.3851C>G
|
ENSP00000055163.8:p.Thr1284Ser
|
|
ENST00000414678.8:c.3920C>G
|
ENSP00000412835.3:p.Thr1307Ser
|
|
ENST00000637015.2:c.4139C>G
|
ENSP00000489729.2:p.Thr1380Ser
|
|
ENST00000346085.10:c.3890C>G
|
ENSP00000344546.5:p.Thr1297Ser
|
|
ENST00000350026.10:c.3602C>G
|
ENSP00000055163.7:p.Thr1201Ser
|
|
ENST00000414678.7:c.2168C>G
|
ENSP00000412835.2:p.Thr723Ser
|
|
ENST00000635849.1:c.1331C>G
|
ENSP00000490948.1:p.Thr444Ser
|
|
ENST00000635957.1:c.965C>G
|
ENSP00000490385.1:p.Thr322Ser
|
|
ENST00000636930.2:c.4010C>G
MANE Select
|
ENSP00000490491.2:p.Thr1337Ser
|
|
ENST00000636940.1:n.2007C>G
|
|
|
ENST00000637015.1:c.1378C>G
|
|
|
ENST00000637568.1:c.1292C>G
|
|
|
ENST00000637741.1:n.676C>G
|
|
|
ENST00000637810.1:c.1352C>G
|
ENSP00000489636.1:p.Thr451Ser
|
|
ENST00000637904.1:c.1511C>G
|
ENSP00000490550.1:p.Thr504Ser
|
|
ENST00000647938.1:c.3641C>G
|
ENSP00000498155.1:p.Thr1214Ser
|
|
ENST00000346085.9:c.3641C>G
|
ENSP00000344546.4:p.Thr1214Ser
|
|
ENST00000350026.9:c.3602C>G
|
ENSP00000055163.7:p.Thr1201Ser
|
|
ENST00000414678.6:c.2168C>G
|
ENSP00000412835.2:p.Thr723Ser
|
|
NM_017519.2:c.3602C>G
|
NP_059989.2:p.Thr1201Ser
|
|
NM_020732.3:c.3641C>G
|
NP_065783.3:p.Thr1214Ser
|
|
XM_005267069.3:c.3761C>G
|
XP_005267126.2:p.Thr1254Ser
|
|
XM_011535984.1:c.2840C>G
|
XP_011534286.1:p.Thr947Ser
|
|
XM_011535985.1:c.2660C>G
|
XP_011534287.1:p.Thr887Ser
|
|
XM_011535986.1:c.2420C>G
|
XP_011534288.1:p.Thr807Ser
|
|
XM_011535987.1:c.2039C>G
|
XP_011534289.1:p.Thr680Ser
|
|
XM_011535988.1:c.902C>G
|
XP_011534290.1:p.Thr301Ser
|
|
NM_001346813.1:c.3761C>G
|
NP_001333742.1:p.Thr1254Ser
|
|
NM_001363725.1:c.1511C>G
|
NP_001350654.1:p.Thr504Ser
|
|
XM_011535984.2:c.3971C>G
|
XP_011534286.2:p.Thr1324Ser
|
|
XM_011535988.3:c.902C>G
|
XP_011534290.1:p.Thr301Ser
|
|
XM_017011103.2:c.3872C>G
|
XP_016866592.1:p.Thr1291Ser
|
|
XM_017011104.1:c.3842C>G
|
XP_016866593.1:p.Thr1281Ser
|
|
XM_017011105.2:c.3812C>G
|
XP_016866594.1:p.Thr1271Ser
|
|
XM_017011106.2:c.3683C>G
|
XP_016866595.1:p.Thr1228Ser
|
|
XM_017011107.2:c.3662C>G
|
XP_016866596.1:p.Thr1221Ser
|
|
XR_002956289.1:n.4054C>G
|
|
|
NM_001363725.2:c.1511C>G
|
NP_001350654.1:p.Thr504Ser
|
|
NM_001371656.1:c.3890C>G
|
NP_001358585.1:p.Thr1297Ser
|
|
NM_001374820.1:c.3890C>G
|
NP_001361749.1:p.Thr1297Ser
|
|
NM_001374828.1:c.4010C>G
MANE Select
|
NP_001361757.1:p.Thr1337Ser
|
|
NM_017519.3:c.3851C>G
|
NP_059989.3:p.Thr1284Ser
|
|