ENST00000578493.2:n.719C>A
|
|
|
ENST00000699291.1:c.511C>A
|
ENSP00000514272.1:p.Pro171Thr
|
|
ENST00000699292.1:n.426C>A
|
|
|
ENST00000225275.4:c.1386C>A
MANE Select
|
ENSP00000225275.3:p.Tyr462Ter
|
|
ENST00000225275.3:c.1386C>A
|
ENSP00000225275.3:p.Tyr462Ter
|
|
NM_000250.1:c.1386C>A , LRG_84t1:c.1386C>A
|
NP_000241.1:p.Tyr462Ter
|
|
XM_011524821.1:c.1572C>A
|
XP_011523123.1:p.Tyr524Ter
|
|
XM_011524822.1:c.1101C>A
|
XP_011523124.1:p.Tyr367Ter
|
|
XM_011524823.1:c.1411C>A
|
XP_011523125.1:p.Pro471Thr
|
|
NM_000250.2:c.1386C>A
MANE Select
|
NP_000241.1:p.Tyr462Ter
|
|