ENST00000290866.10:c.3717C>T
MANE Select
|
ENSP00000290866.4:p.Asp1239=
|
|
ENST00000290863.10:c.1995C>T
|
ENSP00000290863.6:p.Asp665=
|
|
ENST00000290866.9:c.3717C>T
|
ENSP00000290866.4:p.Asp1239=
|
|
ENST00000413513.7:c.1872C>T
|
ENSP00000392247.3:p.Asp624=
|
|
ENST00000428043.5:c.*139C>T
|
ENSP00000397593.2:n.*139C>T
|
|
ENST00000577418.5:n.727C>T
|
|
|
ENST00000577647.2:c.1969+177C>T
|
ENSP00000464149.1:n.1969+177C>T
|
|
ENST00000578839.5:c.*1472C>T
|
ENSP00000462110.2:n.*1472C>T
|
|
ENST00000579314.5:c.*1446C>T
|
ENSP00000462599.1:n.*1446C>T
|
|
NM_000789.3:c.3717C>T
|
NP_000780.1:p.Asp1239=
|
|
NM_001178057.1:c.1872C>T
|
NP_001171528.1:p.Asp624=
|
|
NM_152830.2:c.1995C>T
|
NP_690043.1:p.Asp665=
|
|
XM_005257110.1:c.3168C>T
|
XP_005257167.1:p.Asp1056=
|
|
XM_006721737.2:c.2055C>T
|
XP_006721800.2:p.Asp685=
|
|
XM_006721737.3:c.2055C>T
|
XP_006721800.2:p.Asp685=
|
|
NM_000789.4:c.3717C>T
MANE Select
|
NP_000780.1:p.Asp1239=
|
|
NM_001178057.2:c.1872C>T
|
NP_001171528.1:p.Asp624=
|
|
NM_152830.3:c.1995C>T
|
NP_690043.1:p.Asp665=
|
|
NM_001382700.1:c.3150C>T
|
NP_001369629.1:p.Asp1050=
|
|
NM_001382701.1:c.2865C>T
|
NP_001369630.1:p.Asp955=
|
|
NM_001382702.1:c.1332C>T
|
NP_001369631.1:p.Asp444=
|
|
NR_168483.1:n.2095C>T
|
|
|