ENST00000358807.8:c.3171C>T
MANE Select
|
ENSP00000351664.3:p.Ser1057=
|
|
ENST00000358577.7:c.2913C>T
|
ENSP00000351385.3:p.Ser971=
|
|
ENST00000358807.7:c.3171C>T
|
ENSP00000351664.3:p.Ser1057=
|
|
ENST00000456101.6:n.3950C>T
|
|
|
ENST00000465904.1:n.4222C>T
|
|
|
ENST00000630715.2:c.3228C>T
|
ENSP00000486901.1:p.Ser1076=
|
|
NM_001159291.1:c.2913C>T
|
NP_001152763.1:p.Ser971=
|
|
NM_001286613.1:c.3228C>T
|
NP_001273542.1:p.Ser1076=
|
|
NM_022765.3:c.3171C>T
|
NP_073602.3:p.Ser1057=
|
|
NM_022765.4:c.3171C>T
MANE Select
|
NP_073602.3:p.Ser1057=
|
|
NM_001159291.2:c.2913C>T
|
NP_001152763.1:p.Ser971=
|
|
NM_001286613.2:c.3228C>T
|
NP_001273542.1:p.Ser1076=
|
|