ENST00000369538.4:c.482A>G
|
ENSP00000358551.4:p.Tyr161Cys
|
|
ENST00000520113.7:c.494A>G
MANE Select
|
ENSP00000430075.3:p.Tyr165Cys
|
|
ENST00000637080.1:c.497A>G
|
ENSP00000489753.1:p.Tyr166Cys
|
|
ENST00000639077.1:n.159A>G
|
|
|
ENST00000369538.3:c.581A>G
|
ENSP00000358551.3:p.Tyr194Cys
|
|
ENST00000485564.3:n.368A>G
|
|
|
ENST00000520113.6:c.593A>G
|
ENSP00000430075.2:p.Tyr198Cys
|
|
NM_000036.2:c.593A>G
|
NP_000027.2:p.Tyr198Cys
|
|
NM_001172626.1:c.581A>G
|
NP_001166097.1:p.Tyr194Cys
|
|
NM_000036.3:c.494A>G
MANE Select
|
NP_000027.3:p.Tyr165Cys
|
|
NM_001172626.2:c.482A>G
|
NP_001166097.2:p.Tyr161Cys
|
|