ENST00000251654.9:c.503A>C
MANE Select
|
ENSP00000251654.4:p.Glu168Ala
|
|
ENST00000251654.8:c.503A>C
|
ENSP00000251654.4:p.Glu168Ala
|
|
ENST00000459873.1:c.254A>C
|
ENSP00000419293.1:p.Glu85Ala
|
|
ENST00000462542.5:c.370A>C
|
|
|
ENST00000462637.5:c.434A>C
|
ENSP00000420391.1:p.Glu145Ala
|
|
ENST00000465176.5:n.465A>C
|
|
|
ENST00000466072.5:c.503A>C
|
ENSP00000420158.1:p.Glu168Ala
|
|
ENST00000468777.5:c.596A>C
|
ENSP00000419129.1:p.Glu199Ala
|
|
ENST00000469217.5:c.563A>C
|
ENSP00000419027.1:p.Glu188Ala
|
|
ENST00000471595.5:c.503A>C
|
ENSP00000417549.1:p.Glu168Ala
|
|
ENST00000473073.1:n.460A>C
|
|
|
ENST00000474833.5:n.168+11467A>C
|
|
|
ENST00000475214.5:n.417A>C
|
|
|
ENST00000478469.5:c.503A>C
|
ENSP00000420759.1:p.Glu168Ala
|
|
ENST00000482086.5:c.155A>C
|
ENSP00000417253.1:p.Glu52Ala
|
|
ENST00000483687.5:c.446A>C
|
ENSP00000420639.1:p.Glu149Ala
|
|
ENST00000484181.5:c.503A>C
|
ENSP00000417937.1:p.Glu168Ala
|
|
ENST00000490504.5:c.372+5402A>C
|
ENSP00000418307.1:n.372+5402A>C
|
|
ENST00000494742.5:c.254A>C
|
|
|
NM_000532.4:c.503A>C
|
NP_000523.2:p.Glu168Ala
|
|
NM_001178014.1:c.563A>C
|
NP_001171485.1:p.Glu188Ala
|
|
XM_011512873.1:c.503A>C
|
XP_011511175.1:p.Glu168Ala
|
|
XM_011512873.2:c.503A>C
|
XP_011511175.1:p.Glu168Ala
|
|
NM_000532.5:c.503A>C
MANE Select
|
NP_000523.2:p.Glu168Ala
|
|
NM_001178014.2:c.563A>C
|
NP_001171485.1:p.Glu188Ala
|
|