ENST00000369538.4:c.482A>C
|
ENSP00000358551.4:p.Tyr161Ser
|
|
ENST00000520113.7:c.494A>C
MANE Select
|
ENSP00000430075.3:p.Tyr165Ser
|
|
ENST00000637080.1:c.497A>C
|
ENSP00000489753.1:p.Tyr166Ser
|
|
ENST00000639077.1:n.159A>C
|
|
|
ENST00000369538.3:c.581A>C
|
ENSP00000358551.3:p.Tyr194Ser
|
|
ENST00000485564.3:n.368A>C
|
|
|
ENST00000520113.6:c.593A>C
|
ENSP00000430075.2:p.Tyr198Ser
|
|
NM_000036.2:c.593A>C
|
NP_000027.2:p.Tyr198Ser
|
|
NM_001172626.1:c.581A>C
|
NP_001166097.1:p.Tyr194Ser
|
|
NM_000036.3:c.494A>C
MANE Select
|
NP_000027.3:p.Tyr165Ser
|
|
NM_001172626.2:c.482A>C
|
NP_001166097.2:p.Tyr161Ser
|
|