ENST00000219097.7:c.369C>A
MANE Select
|
ENSP00000219097.2:p.Ser123=
|
|
ENST00000219097.6:c.369C>A
|
ENSP00000219097.2:p.Ser123=
|
|
ENST00000563306.5:n.452C>A
|
|
|
ENST00000563599.5:c.*191C>A
|
ENSP00000454299.1:n.*191C>A
|
|
ENST00000566860.1:c.222C>A
|
ENSP00000456981.1:p.Ser74=
|
|
ENST00000568364.6:c.369C>A
|
ENSP00000457282.2:p.Ser123=
|
|
ENST00000569239.5:n.416C>A
|
|
|
ENST00000570260.2:n.368C>A
|
|
|
NM_014321.3:c.369C>A
|
NP_055136.1:p.Ser123=
|
|
NR_037620.1:n.488C>A
|
|
|
XM_011522978.1:c.369C>A
|
XP_011521280.1:p.Ser123=
|
|
XM_011522978.3:c.369C>A
|
XP_011521280.1:p.Ser123=
|
|
NM_014321.4:c.369C>A
MANE Select
|
NP_055136.1:p.Ser123=
|
|
NR_037620.2:n.475C>A
|
|
|