ENST00000412167.7:c.2529G=
|
ENSP00000390987.3:p.Thr843=
|
|
ENST00000684818.1:n.1233G=
|
|
|
ENST00000685269.1:n.2619G=
|
|
|
ENST00000686011.1:c.2526G=
|
ENSP00000509704.1:p.Thr842=
|
|
ENST00000687109.1:c.2544G=
|
ENSP00000509371.1:p.Thr848=
|
|
ENST00000687208.1:n.2953G=
|
|
|
ENST00000687246.1:c.2406G=
|
ENSP00000509114.1:p.Thr802=
|
|
ENST00000687265.1:n.2699G=
|
|
|
ENST00000687295.1:c.2529G=
|
ENSP00000509450.1:p.Thr843=
|
|
ENST00000688060.1:n.338G=
|
|
|
ENST00000689832.1:c.2541G=
|
ENSP00000509084.1:p.Thr847=
|
|
ENST00000689994.1:c.2031G=
|
ENSP00000509156.1:p.Thr677=
|
|
ENST00000690543.1:c.2532G=
|
ENSP00000508831.1:p.Thr844=
|
|
ENST00000690917.1:n.2759G=
|
|
|
ENST00000691361.1:n.1451G=
|
|
|
ENST00000692301.1:n.1233G=
|
|
|
ENST00000692783.1:c.2538G=
|
ENSP00000508733.1:p.Thr846=
|
|
ENST00000692991.1:n.2638G=
|
|
|
ENST00000288135.6:c.2541G=
MANE Select
|
ENSP00000288135.6:p.Thr847=
|
|
ENST00000288135.5:c.2541G=
|
ENSP00000288135.5:p.Thr847=
|
|
ENST00000412167.6:c.2529G=
|
ENSP00000390987.2:p.Thr843=
|
|
NM_000222.2:c.2541G= , LRG_307t1:c.2541G=
|
NP_000213.1:p.Thr847=
|
|
NM_001093772.1:c.2529G=
|
NP_001087241.1:p.Thr843=
|
|
XM_005265740.1:c.2544G=
|
XP_005265797.1:p.Thr848=
|
|
XM_005265741.1:c.2541G=
|
XP_005265798.1:p.Thr847=
|
|
XM_005265742.1:c.2532G=
|
XP_005265799.1:p.Thr844=
|
|
XM_005265742.3:c.2532G=
|
XP_005265799.1:p.Thr844=
|
|
XM_017008178.1:c.2538G=
|
XP_016863667.1:p.Thr846=
|
|
XM_017008179.1:c.2529G=
|
XP_016863668.1:p.Thr843=
|
|
XM_017008180.1:c.2526G=
|
XP_016863669.1:p.Thr842=
|
|
NM_000222.3:c.2541G=
MANE Select
|
NP_000213.1:p.Thr847=
|
|
NM_001093772.2:c.2529G=
|
NP_001087241.1:p.Thr843=
|
|
NM_001385284.1:c.2544G=
|
NP_001372213.1:p.Thr848=
|
|
NM_001385285.1:c.2538G=
|
NP_001372214.1:p.Thr846=
|
|
NM_001385286.1:c.2526G=
|
NP_001372215.1:p.Thr842=
|
|
NM_001385288.1:c.2532G=
|
NP_001372217.1:p.Thr844=
|
|
NM_001385290.1:c.2541G=
|
NP_001372219.1:p.Thr847=
|
|
NM_001385292.1:c.2529G=
|
NP_001372221.1:p.Thr843=
|
|