ENST00000578493.2:n.801A>T
|
|
|
ENST00000699291.1:c.593A>T
|
ENSP00000514272.1:n.593A>T
|
|
ENST00000699292.1:n.508A>T
|
|
|
ENST00000225275.4:c.1468A>T
MANE Select
|
ENSP00000225275.3:p.Ile490Phe
|
|
ENST00000225275.3:c.1468A>T
|
ENSP00000225275.3:p.Ile490Phe
|
|
NM_000250.1:c.1468A>T , LRG_84t1:c.1468A>T
|
NP_000241.1:p.Ile490Phe
|
|
XM_011524821.1:c.1654A>T
|
XP_011523123.1:p.Ile552Phe
|
|
XM_011524822.1:c.1183A>T
|
XP_011523124.1:p.Ile395Phe
|
|
XM_011524823.1:c.*17A>T
|
XP_011523125.1:n.*17A>T
|
|
NM_000250.2:c.1468A>T
MANE Select
|
NP_000241.1:p.Ile490Phe
|
|