ENST00000355832.10:c.4063G>A
MANE Select
|
ENSP00000348089.5:p.Asp1355Asn
|
|
ENST00000679552.1:n.2272G>A
|
|
|
ENST00000679871.1:n.1209G>A
|
|
|
ENST00000679974.1:n.1112G>A
|
|
|
ENST00000681632.1:n.5466G>A
|
|
|
ENST00000681659.1:c.3904G>A
|
ENSP00000505631.1:p.Asp1302Asn
|
|
ENST00000355832.9:c.4063G>A
|
ENSP00000348089.5:p.Asp1355Asn
|
|
ENST00000623073.3:c.*2359G>A
|
ENSP00000485650.1:n.*2359G>A
|
|
ENST00000623115.3:c.2173G>A
|
ENSP00000485321.1:p.Asp725Asn
|
|
ENST00000624341.3:c.1895G>A
|
|
|
NM_000124.3:c.4063G>A
|
NP_000115.1:p.Asp1355Asn
|
|
XR_945953.1:n.243-12331C>T
|
|
|
NM_001346440.1:c.4063G>A
|
NP_001333369.1:p.Asp1355Asn
|
|
NM_000124.4:c.4063G>A
MANE Select
|
NP_000115.1:p.Asp1355Asn
|
|
NM_001346440.2:c.4063G>A
|
NP_001333369.1:p.Asp1355Asn
|
|