ENST00000251654.9:c.478G>C
MANE Select
|
ENSP00000251654.4:p.Asp160His
|
|
ENST00000251654.8:c.478G>C
|
ENSP00000251654.4:p.Asp160His
|
|
ENST00000459873.1:c.229G>C
|
ENSP00000419293.1:p.Asp77His
|
|
ENST00000462542.5:c.345G>C
|
|
|
ENST00000462637.5:c.409G>C
|
ENSP00000420391.1:p.Asp137His
|
|
ENST00000465176.5:n.440G>C
|
|
|
ENST00000465423.5:c.565G>C
|
ENSP00000419263.1:p.Asp189His
|
|
ENST00000466072.5:c.478G>C
|
ENSP00000420158.1:p.Asp160His
|
|
ENST00000468777.5:c.571G>C
|
ENSP00000419129.1:p.Asp191His
|
|
ENST00000469217.5:c.538G>C
|
ENSP00000419027.1:p.Asp180His
|
|
ENST00000471595.5:c.478G>C
|
ENSP00000417549.1:p.Asp160His
|
|
ENST00000473073.1:n.435G>C
|
|
|
ENST00000474833.5:n.168+11442G>C
|
|
|
ENST00000475214.5:n.392G>C
|
|
|
ENST00000478469.5:c.478G>C
|
ENSP00000420759.1:p.Asp160His
|
|
ENST00000482086.5:c.130G>C
|
ENSP00000417253.1:p.Asp44His
|
|
ENST00000483687.5:c.421G>C
|
ENSP00000420639.1:p.Asp141His
|
|
ENST00000484181.5:c.478G>C
|
ENSP00000417937.1:p.Asp160His
|
|
ENST00000490504.5:c.372+5377G>C
|
ENSP00000418307.1:n.372+5377G>C
|
|
ENST00000494742.5:c.229G>C
|
ENSP00000418020.1:p.Asp77His
|
|
NM_000532.4:c.478G>C
|
NP_000523.2:p.Asp160His
|
|
NM_001178014.1:c.538G>C
|
NP_001171485.1:p.Asp180His
|
|
XM_011512873.1:c.478G>C
|
XP_011511175.1:p.Asp160His
|
|
XM_011512873.2:c.478G>C
|
XP_011511175.1:p.Asp160His
|
|
NM_000532.5:c.478G>C
MANE Select
|
NP_000523.2:p.Asp160His
|
|
NM_001178014.2:c.538G>C
|
NP_001171485.1:p.Asp180His
|
|