ENST00000369538.4:c.524G=
|
ENSP00000358551.4:p.Ser175=
|
|
ENST00000520113.7:c.536G=
MANE Select
|
ENSP00000430075.3:p.Ser179=
|
|
ENST00000637080.1:c.539G=
|
ENSP00000489753.1:p.Ser180=
|
|
ENST00000639077.1:n.201G=
|
|
|
ENST00000369538.3:c.623G=
|
ENSP00000358551.3:p.Ser208=
|
|
ENST00000485564.3:n.410G=
|
|
|
ENST00000520113.6:c.635G=
|
ENSP00000430075.2:p.Ser212=
|
|
NM_000036.2:c.635G=
|
NP_000027.2:p.Ser212=
|
|
NM_001172626.1:c.623G=
|
NP_001166097.1:p.Ser208=
|
|
NM_000036.3:c.536G=
MANE Select
|
NP_000027.3:p.Ser179=
|
|
NM_001172626.2:c.524G=
|
NP_001166097.2:p.Ser175=
|
|