ENST00000355832.10:c.3532T>A
MANE Select
|
ENSP00000348089.5:p.Phe1178Ile
|
|
ENST00000679552.1:n.603T>A
|
|
|
ENST00000679871.1:n.678T>A
|
|
|
ENST00000679974.1:n.581T>A
|
|
|
ENST00000681632.1:n.4935T>A
|
|
|
ENST00000681659.1:c.3373T>A
|
ENSP00000505631.1:p.Phe1125Ile
|
|
ENST00000355832.9:c.3532T>A
|
ENSP00000348089.5:p.Phe1178Ile
|
|
ENST00000623073.3:c.*1828T>A
|
ENSP00000485650.1:n.*1828T>A
|
|
ENST00000623115.3:c.1642T>A
|
ENSP00000485321.1:p.Phe548Ile
|
|
ENST00000624341.3:c.1364T>A
|
|
|
NM_000124.3:c.3532T>A
|
NP_000115.1:p.Phe1178Ile
|
|
XR_945953.1:n.243-1137A>T
|
|
|
NM_001346440.1:c.3532T>A
|
NP_001333369.1:p.Phe1178Ile
|
|
NM_000124.4:c.3532T>A
MANE Select
|
NP_000115.1:p.Phe1178Ile
|
|
NM_001346440.2:c.3532T>A
|
NP_001333369.1:p.Phe1178Ile
|
|