ENST00000361418.10:c.4196C>G
MANE Select
|
ENSP00000354878.5:p.Thr1399Ser
|
|
ENST00000636569.1:c.4133C>G
|
ENSP00000490369.1:p.Thr1378Ser
|
|
ENST00000361418.9:c.4196C>G
|
ENSP00000354878.5:p.Thr1399Ser
|
|
ENST00000361961.7:c.4157C>G
|
ENSP00000354851.3:p.Thr1386Ser
|
|
ENST00000541463.6:c.4037C>G
|
ENSP00000438075.2:p.Thr1346Ser
|
|
ENST00000544797.6:c.4085C>G
|
ENSP00000445606.2:p.Thr1362Ser
|
|
ENST00000547733.1:n.1510C>G
|
|
|
ENST00000551264.5:c.1139C>G
|
ENSP00000448792.1:p.Thr380Ser
|
|
ENST00000552961.5:c.2098C>G
|
|
|
NM_001173463.1:c.4085C>G
|
NP_001166934.1:p.Thr1362Ser
|
|
NM_001173464.1:c.4196C>G
|
NP_001166935.1:p.Thr1399Ser
|
|
NM_001173465.1:c.4037C>G
|
NP_001166936.1:p.Thr1346Ser
|
|
NM_017641.3:c.4157C>G
|
NP_060111.2:p.Thr1386Ser
|
|
XM_005269007.1:c.4199C>G
|
XP_005269064.1:p.Thr1400Ser
|
|
XM_005269008.1:c.4184C>G
|
XP_005269065.1:p.Thr1395Ser
|
|
XM_005269009.1:c.4178C>G
|
XP_005269066.1:p.Thr1393Ser
|
|
XM_005269010.1:c.4160C>G
|
XP_005269067.1:p.Thr1387Ser
|
|
XM_005269011.1:c.4145C>G
|
XP_005269068.1:p.Thr1382Ser
|
|
XM_005269012.1:c.4070C>G
|
XP_005269069.1:p.Thr1357Ser
|
|
XM_005269013.1:c.4055C>G
|
XP_005269070.1:p.Thr1352Ser
|
|
XM_005269014.1:c.4016C>G
|
XP_005269071.1:p.Thr1339Ser
|
|
XM_006719493.1:c.4139C>G
|
XP_006719556.1:p.Thr1380Ser
|
|
XM_006719494.1:c.4067C>G
|
XP_006719557.1:p.Thr1356Ser
|
|
XM_006719496.1:c.4124C>G
|
XP_006719559.1:p.Thr1375Ser
|
|
XM_011538556.1:c.4130C>G
|
XP_011536858.1:p.Thr1377Ser
|
|
XM_005269007.3:c.4199C>G
|
XP_005269064.1:p.Thr1400Ser
|
|
XM_005269008.3:c.4184C>G
|
XP_005269065.1:p.Thr1395Ser
|
|
XM_005269009.3:c.4178C>G
|
XP_005269066.1:p.Thr1393Ser
|
|
XM_005269010.3:c.4160C>G
|
XP_005269067.1:p.Thr1387Ser
|
|
XM_005269011.3:c.4145C>G
|
XP_005269068.1:p.Thr1382Ser
|
|
XM_005269012.3:c.4070C>G
|
XP_005269069.1:p.Thr1357Ser
|
|
XM_005269013.3:c.4055C>G
|
XP_005269070.1:p.Thr1352Ser
|
|
XM_005269014.3:c.4016C>G
|
XP_005269071.1:p.Thr1339Ser
|
|
XM_006719493.3:c.4139C>G
|
XP_006719556.1:p.Thr1380Ser
|
|
XM_006719494.3:c.4067C>G
|
XP_006719557.1:p.Thr1356Ser
|
|
XM_011538556.3:c.4130C>G
|
XP_011536858.1:p.Thr1377Ser
|
|
XM_017019607.2:c.4145C>G
|
XP_016875096.1:p.Thr1382Ser
|
|
XM_017019608.2:c.4106C>G
|
XP_016875097.1:p.Thr1369Ser
|
|
XM_017019609.2:c.3995C>G
|
XP_016875098.1:p.Thr1332Ser
|
|
XM_017019610.2:c.3995C>G
|
XP_016875099.1:p.Thr1332Ser
|
|
XM_017019611.2:c.3977C>G
|
XP_016875100.1:p.Thr1326Ser
|
|
NM_001173463.2:c.4085C>G
|
NP_001166934.1:p.Thr1362Ser
|
|
NM_001173464.2:c.4196C>G
MANE Select
|
NP_001166935.1:p.Thr1399Ser
|
|
NM_001173465.2:c.4037C>G
|
NP_001166936.1:p.Thr1346Ser
|
|
NM_017641.4:c.4157C>G
|
NP_060111.2:p.Thr1386Ser
|
|
NM_001378439.1:c.4199C>G
|
NP_001365368.1:p.Thr1400Ser
|
|
NM_001378440.1:c.4184C>G
|
NP_001365369.1:p.Thr1395Ser
|
|
NM_001378441.1:c.4160C>G
|
NP_001365370.1:p.Thr1387Ser
|
|