ENST00000369538.4:c.496G>A
|
ENSP00000358551.4:p.Asp166Asn
|
|
ENST00000520113.7:c.508G>A
MANE Select
|
ENSP00000430075.3:p.Asp170Asn
|
|
ENST00000637080.1:c.511G>A
|
ENSP00000489753.1:p.Asp171Asn
|
|
ENST00000639077.1:n.173G>A
|
|
|
ENST00000369538.3:c.595G>A
|
ENSP00000358551.3:p.Asp199Asn
|
|
ENST00000485564.3:n.382G>A
|
|
|
ENST00000520113.6:c.607G>A
|
ENSP00000430075.2:p.Asp203Asn
|
|
NM_000036.2:c.607G>A
|
NP_000027.2:p.Asp203Asn
|
|
NM_001172626.1:c.595G>A
|
NP_001166097.1:p.Asp199Asn
|
|
NM_000036.3:c.508G>A
MANE Select
|
NP_000027.3:p.Asp170Asn
|
|
NM_001172626.2:c.496G>A
|
NP_001166097.2:p.Asp166Asn
|
|