ENST00000578493.2:n.753A>T
|
|
|
ENST00000699291.1:c.545A>T
|
ENSP00000514272.1:p.Glu182Val
|
|
ENST00000699292.1:n.460A>T
|
|
|
ENST00000225275.4:c.1420A>T
MANE Select
|
ENSP00000225275.3:p.Lys474Ter
|
|
ENST00000225275.3:c.1420A>T
|
ENSP00000225275.3:p.Lys474Ter
|
|
NM_000250.1:c.1420A>T , LRG_84t1:c.1420A>T
|
NP_000241.1:p.Lys474Ter
|
|
XM_011524821.1:c.1606A>T
|
XP_011523123.1:p.Lys536Ter
|
|
XM_011524822.1:c.1135A>T
|
XP_011523124.1:p.Lys379Ter
|
|
XM_011524823.1:c.1445A>T
|
XP_011523125.1:p.Glu482Val
|
|
NM_000250.2:c.1420A>T
MANE Select
|
NP_000241.1:p.Lys474Ter
|
|