ENST00000350026.11:c.3878T>C
|
ENSP00000055163.8:p.Met1293Thr
|
|
ENST00000414678.8:c.3947T>C
|
ENSP00000412835.3:p.Met1316Thr
|
|
ENST00000637015.2:c.4166T>C
|
ENSP00000489729.2:p.Met1389Thr
|
|
ENST00000346085.10:c.3917T>C
|
ENSP00000344546.5:p.Met1306Thr
|
|
ENST00000350026.10:c.3629T>C
|
ENSP00000055163.7:p.Met1210Thr
|
|
ENST00000414678.7:c.2195T>C
|
ENSP00000412835.2:p.Met732Thr
|
|
ENST00000635849.1:c.1358T>C
|
ENSP00000490948.1:p.Met453Thr
|
|
ENST00000635957.1:c.992T>C
|
ENSP00000490385.1:p.Met331Thr
|
|
ENST00000636930.2:c.4037T>C
MANE Select
|
ENSP00000490491.2:p.Met1346Thr
|
|
ENST00000636940.1:n.2034T>C
|
|
|
ENST00000637015.1:c.1405T>C
|
|
|
ENST00000637568.1:c.1319T>C
|
|
|
ENST00000637741.1:n.703T>C
|
|
|
ENST00000637810.1:c.1379T>C
|
ENSP00000489636.1:p.Met460Thr
|
|
ENST00000637904.1:c.1538T>C
|
ENSP00000490550.1:p.Met513Thr
|
|
ENST00000647938.1:c.3668T>C
|
ENSP00000498155.1:p.Met1223Thr
|
|
ENST00000346085.9:c.3668T>C
|
ENSP00000344546.4:p.Met1223Thr
|
|
ENST00000350026.9:c.3629T>C
|
ENSP00000055163.7:p.Met1210Thr
|
|
ENST00000414678.6:c.2195T>C
|
ENSP00000412835.2:p.Met732Thr
|
|
NM_017519.2:c.3629T>C
|
NP_059989.2:p.Met1210Thr
|
|
NM_020732.3:c.3668T>C
|
NP_065783.3:p.Met1223Thr
|
|
XM_005267069.3:c.3788T>C
|
XP_005267126.2:p.Met1263Thr
|
|
XM_011535984.1:c.2867T>C
|
XP_011534286.1:p.Met956Thr
|
|
XM_011535985.1:c.2687T>C
|
XP_011534287.1:p.Met896Thr
|
|
XM_011535986.1:c.2447T>C
|
XP_011534288.1:p.Met816Thr
|
|
XM_011535987.1:c.2066T>C
|
XP_011534289.1:p.Met689Thr
|
|
XM_011535988.1:c.929T>C
|
XP_011534290.1:p.Met310Thr
|
|
NM_001346813.1:c.3788T>C
|
NP_001333742.1:p.Met1263Thr
|
|
NM_001363725.1:c.1538T>C
|
NP_001350654.1:p.Met513Thr
|
|
XM_011535984.2:c.3998T>C
|
XP_011534286.2:p.Met1333Thr
|
|
XM_011535988.3:c.929T>C
|
XP_011534290.1:p.Met310Thr
|
|
XM_017011103.2:c.3899T>C
|
XP_016866592.1:p.Met1300Thr
|
|
XM_017011104.1:c.3869T>C
|
XP_016866593.1:p.Met1290Thr
|
|
XM_017011105.2:c.3839T>C
|
XP_016866594.1:p.Met1280Thr
|
|
XM_017011106.2:c.3710T>C
|
XP_016866595.1:p.Met1237Thr
|
|
XM_017011107.2:c.3689T>C
|
XP_016866596.1:p.Met1230Thr
|
|
XR_002956289.1:n.4081T>C
|
|
|
NM_001363725.2:c.1538T>C
|
NP_001350654.1:p.Met513Thr
|
|
NM_001371656.1:c.3917T>C
|
NP_001358585.1:p.Met1306Thr
|
|
NM_001374820.1:c.3917T>C
|
NP_001361749.1:p.Met1306Thr
|
|
NM_001374828.1:c.4037T>C
MANE Select
|
NP_001361757.1:p.Met1346Thr
|
|
NM_017519.3:c.3878T>C
|
NP_059989.3:p.Met1293Thr
|
|