ENST00000369538.4:c.880A>T
|
ENSP00000358551.4:p.Arg294Trp
|
|
ENST00000520113.7:c.892A>T
MANE Select
|
ENSP00000430075.3:p.Arg298Trp
|
|
ENST00000637080.1:c.675A>T
|
ENSP00000489753.1:n.675A>T
|
|
ENST00000639077.1:n.557A>T
|
|
|
ENST00000369538.3:c.979A>T
|
ENSP00000358551.3:p.Arg327Trp
|
|
ENST00000520113.6:c.991A>T
|
ENSP00000430075.2:p.Arg331Trp
|
|
NM_000036.2:c.991A>T
|
NP_000027.2:p.Arg331Trp
|
|
NM_001172626.1:c.979A>T
|
NP_001166097.1:p.Arg327Trp
|
|
NM_000036.3:c.892A>T
MANE Select
|
NP_000027.3:p.Arg298Trp
|
|
NM_001172626.2:c.880A>T
|
NP_001166097.2:p.Arg294Trp
|
|