ENST00000369538.4:c.411T>G
|
ENSP00000358551.4:p.Tyr137Ter
|
|
ENST00000520113.7:c.423T>G
MANE Select
|
ENSP00000430075.3:p.Tyr141Ter
|
|
ENST00000637080.1:c.426T>G
|
ENSP00000489753.1:p.Tyr142Ter
|
|
ENST00000639077.1:n.88T>G
|
|
|
ENST00000369538.3:c.510T>G
|
ENSP00000358551.3:p.Tyr170Ter
|
|
ENST00000485564.3:n.297T>G
|
|
|
ENST00000520113.6:c.522T>G
|
ENSP00000430075.2:p.Tyr174Ter
|
|
NM_000036.2:c.522T>G
|
NP_000027.2:p.Tyr174Ter
|
|
NM_001172626.1:c.510T>G
|
NP_001166097.1:p.Tyr170Ter
|
|
NM_000036.3:c.423T>G
MANE Select
|
NP_000027.3:p.Tyr141Ter
|
|
NM_001172626.2:c.411T>G
|
NP_001166097.2:p.Tyr137Ter
|
|