ENST00000578493.2:n.752G>T
|
|
|
ENST00000699291.1:c.544G>T
|
ENSP00000514272.1:p.Glu182Ter
|
|
ENST00000699292.1:n.459G>T
|
|
|
ENST00000225275.4:c.1419G>T
MANE Select
|
ENSP00000225275.3:p.Arg473Ser
|
|
ENST00000225275.3:c.1419G>T
|
ENSP00000225275.3:p.Arg473Ser
|
|
NM_000250.1:c.1419G>T , LRG_84t1:c.1419G>T
|
NP_000241.1:p.Arg473Ser
|
|
XM_011524821.1:c.1605G>T
|
XP_011523123.1:p.Arg535Ser
|
|
XM_011524822.1:c.1134G>T
|
XP_011523124.1:p.Arg378Ser
|
|
XM_011524823.1:c.1444G>T
|
XP_011523125.1:p.Glu482Ter
|
|
NM_000250.2:c.1419G>T
MANE Select
|
NP_000241.1:p.Arg473Ser
|
|