ENST00000369538.4:c.1273T>A
|
ENSP00000358551.4:p.Tyr425Asn
|
|
ENST00000520113.7:c.1285T>A
MANE Select
|
ENSP00000430075.3:p.Tyr429Asn
|
|
ENST00000637080.1:c.1068T>A
|
ENSP00000489753.1:n.1068T>A
|
|
ENST00000639077.1:n.950T>A
|
|
|
ENST00000369538.3:c.1372T>A
|
ENSP00000358551.3:p.Tyr458Asn
|
|
ENST00000520113.6:c.1384T>A
|
ENSP00000430075.2:p.Tyr462Asn
|
|
NM_000036.2:c.1384T>A
|
NP_000027.2:p.Tyr462Asn
|
|
NM_001172626.1:c.1372T>A
|
NP_001166097.1:p.Tyr458Asn
|
|
NM_000036.3:c.1285T>A
MANE Select
|
NP_000027.3:p.Tyr429Asn
|
|
NM_001172626.2:c.1273T>A
|
NP_001166097.2:p.Tyr425Asn
|
|