ENST00000476680.2:c.579C>G
|
|
|
ENST00000537320.6:c.3476C>G
|
ENSP00000443478.1:p.Thr1159Ser
|
|
ENST00000542877.6:c.4298C>G
|
ENSP00000442242.1:p.Thr1433Ser
|
|
ENST00000705190.1:c.2330C>G
|
ENSP00000516083.1:p.Thr777Ser
|
|
ENST00000705191.1:c.986C>G
|
ENSP00000516084.1:p.Thr329Ser
|
|
ENST00000705192.1:c.4345C>G
|
|
|
ENST00000350763.9:c.5387C>G
MANE Select
|
ENSP00000265131.4:p.Thr1796Ser
|
|
ENST00000341037.8:c.4841C>G
|
ENSP00000339553.4:p.Thr1614Ser
|
|
ENST00000350763.8:c.5387C>G
|
ENSP00000265131.4:p.Thr1796Ser
|
|
ENST00000423613.6:c.4568C>G
|
ENSP00000411406.2:p.Thr1523Ser
|
|
ENST00000476680.1:n.514C>G
|
|
|
ENST00000498724.5:n.301C>G
|
|
|
ENST00000535648.5:c.4298C>G
|
ENSP00000438152.2:p.Thr1433Ser
|
|
ENST00000537320.5:c.3476C>G
|
ENSP00000443478.1:p.Thr1159Ser
|
|
ENST00000542877.5:c.4298C>G
|
ENSP00000442242.1:p.Thr1433Ser
|
|
ENST00000544972.1:c.1074C>G
|
|
|
NM_002160.3:c.5387C>G
|
NP_002151.2:p.Thr1796Ser
|
|
XM_005251972.2:c.5114C>G
|
XP_005252029.1:p.Thr1705Ser
|
|
XM_005251973.2:c.4295C>G
|
XP_005252030.1:p.Thr1432Ser
|
|
XM_005251974.2:c.3749C>G
|
XP_005252031.1:p.Thr1250Ser
|
|
XM_005251975.2:c.3476C>G
|
XP_005252032.1:p.Thr1159Ser
|
|
XM_006717096.2:c.5663C>G
|
XP_006717159.1:p.Thr1888Ser
|
|
XM_006717097.2:c.5114C>G
|
XP_006717160.1:p.Thr1705Ser
|
|
XM_006717098.2:c.4841C>G
|
XP_006717161.1:p.Thr1614Ser
|
|
XM_006717100.2:c.4568C>G
|
XP_006717163.1:p.Thr1523Ser
|
|
XM_006717101.2:c.3749C>G
|
XP_006717164.1:p.Thr1250Ser
|
|
XM_011518622.1:c.5390C>G
|
XP_011516924.1:p.Thr1797Ser
|
|
XM_011518623.1:c.5390C>G
|
XP_011516925.1:p.Thr1797Ser
|
|
XM_011518624.1:c.4844C>G
|
XP_011516926.1:p.Thr1615Ser
|
|
XM_011518625.1:c.4841C>G
|
XP_011516927.1:p.Thr1614Ser
|
|
XM_011518626.1:c.4571C>G
|
XP_011516928.1:p.Thr1524Ser
|
|
XM_011518627.1:c.4298C>G
|
XP_011516929.1:p.Thr1433Ser
|
|
XM_011518628.1:c.4022C>G
|
XP_011516930.1:p.Thr1341Ser
|
|
XM_011518629.1:c.4022C>G
|
XP_011516931.1:p.Thr1341Ser
|
|
XM_005251972.4:c.5114C>G
|
XP_005252029.1:p.Thr1705Ser
|
|
XM_005251973.4:c.4295C>G
|
XP_005252030.1:p.Thr1432Ser
|
|
XM_005251974.4:c.3749C>G
|
XP_005252031.1:p.Thr1250Ser
|
|
XM_005251975.4:c.3476C>G
|
XP_005252032.1:p.Thr1159Ser
|
|
XM_006717096.4:c.5663C>G
|
XP_006717159.1:p.Thr1888Ser
|
|
XM_006717097.4:c.5114C>G
|
XP_006717160.1:p.Thr1705Ser
|
|
XM_006717098.4:c.4841C>G
|
XP_006717161.1:p.Thr1614Ser
|
|
XM_006717101.4:c.3749C>G
|
XP_006717164.1:p.Thr1250Ser
|
|
XM_011518625.3:c.4841C>G
|
XP_011516927.1:p.Thr1614Ser
|
|
XM_011518626.3:c.4571C>G
|
XP_011516928.1:p.Thr1524Ser
|
|
XM_011518628.3:c.4022C>G
|
XP_011516930.1:p.Thr1341Ser
|
|
XM_011518629.3:c.4022C>G
|
XP_011516931.1:p.Thr1341Ser
|
|
XM_017014678.2:c.5936C>G
|
XP_016870167.1:p.Thr1979Ser
|
|
XM_017014679.2:c.5663C>G
|
XP_016870168.1:p.Thr1888Ser
|
|
XM_017014680.2:c.5660C>G
|
XP_016870169.1:p.Thr1887Ser
|
|
XM_017014681.2:c.4844C>G
|
XP_016870170.1:p.Thr1615Ser
|
|
XM_024447530.1:c.5936C>G
|
XP_024303298.1:p.Thr1979Ser
|
|
NM_002160.4:c.5387C>G
MANE Select
|
NP_002151.2:p.Thr1796Ser
|
|