ENST00000455537.7:c.2930G=
MANE Select
|
ENSP00000408979.2:p.Ser977=
|
|
ENST00000674619.1:c.2951G=
|
ENSP00000502270.1:p.Ser984=
|
|
ENST00000675697.1:c.21G=
|
|
|
ENST00000675737.1:n.334G=
|
|
|
ENST00000675882.1:n.2453G=
|
|
|
ENST00000675929.1:n.1488G=
|
|
|
ENST00000676055.1:c.21G=
|
|
|
ENST00000676457.1:c.2825G=
|
ENSP00000501588.1:p.Ser942=
|
|
ENST00000286452.5:c.2663G=
|
ENSP00000286452.5:p.Ser888=
|
|
ENST00000455537.6:c.2930G=
|
ENSP00000408979.2:p.Ser977=
|
|
ENST00000552227.1:n.213G=
|
|
|
NM_004984.2:c.2930G=
|
NP_004975.2:p.Ser977=
|
|
NM_001354705.1:c.2663G=
|
NP_001341634.1:p.Ser888=
|
|
NM_004984.3:c.2930G=
|
NP_004975.2:p.Ser977=
|
|
XR_002957324.1:n.3163G=
|
|
|
NM_004984.4:c.2930G=
MANE Select
|
NP_004975.2:p.Ser977=
|
|
NM_001354705.2:c.2663G=
|
NP_001341634.1:p.Ser888=
|
|