ENST00000578493.2:n.710C>A
|
|
|
ENST00000699291.1:c.502C>A
|
ENSP00000514272.1:p.Pro168Thr
|
|
ENST00000699292.1:n.417C>A
|
|
|
ENST00000225275.4:c.1377C>A
MANE Select
|
ENSP00000225275.3:p.Tyr459Ter
|
|
ENST00000225275.3:c.1377C>A
|
ENSP00000225275.3:p.Tyr459Ter
|
|
NM_000250.1:c.1377C>A , LRG_84t1:c.1377C>A
|
NP_000241.1:p.Tyr459Ter
|
|
XM_011524821.1:c.1563C>A
|
XP_011523123.1:p.Tyr521Ter
|
|
XM_011524822.1:c.1092C>A
|
XP_011523124.1:p.Tyr364Ter
|
|
XM_011524823.1:c.1402C>A
|
XP_011523125.1:p.Pro468Thr
|
|
NM_000250.2:c.1377C>A
MANE Select
|
NP_000241.1:p.Tyr459Ter
|
|