ENST00000355832.10:c.3705C>T
MANE Select
|
ENSP00000348089.5:p.Asp1235=
|
|
ENST00000679552.1:n.776C>T
|
|
|
ENST00000679871.1:n.851C>T
|
|
|
ENST00000679974.1:n.754C>T
|
|
|
ENST00000681632.1:n.5108C>T
|
|
|
ENST00000681659.1:c.3546C>T
|
ENSP00000505631.1:p.Asp1182=
|
|
ENST00000355832.9:c.3705C>T
|
ENSP00000348089.5:p.Asp1235=
|
|
ENST00000465653.1:n.27C>T
|
|
|
ENST00000623073.3:c.*2001C>T
|
ENSP00000485650.1:n.*2001C>T
|
|
ENST00000623115.3:c.1815C>T
|
ENSP00000485321.1:p.Asp605=
|
|
ENST00000624341.3:c.1537C>T
|
|
|
NM_000124.3:c.3705C>T
|
NP_000115.1:p.Asp1235=
|
|
XR_945953.1:n.243-1310G>A
|
|
|
NM_001346440.1:c.3705C>T
|
NP_001333369.1:p.Asp1235=
|
|
NM_000124.4:c.3705C>T
MANE Select
|
NP_000115.1:p.Asp1235=
|
|
NM_001346440.2:c.3705C>T
|
NP_001333369.1:p.Asp1235=
|
|