ENST00000291295.14:c.255G>T
MANE Select
|
ENSP00000291295.8:p.Glu85Asp
|
|
ENST00000595072.2:n.2684G>T
|
|
|
ENST00000602169.2:c.*291G>T
|
ENSP00000499372.1:n.*291G>T
|
|
ENST00000291295.13:c.255G>T
|
ENSP00000291295.8:p.Glu85Asp
|
|
ENST00000391918.6:c.147G>T
|
ENSP00000375785.2:p.Glu49Asp
|
|
ENST00000477244.5:n.379G>T
|
|
|
ENST00000482455.5:n.365G>T
|
|
|
ENST00000486500.1:n.456G>T
|
|
|
ENST00000594523.5:c.147G>T
|
ENSP00000468877.1:p.Glu49Asp
|
|
ENST00000595072.1:n.445G>T
|
|
|
ENST00000596362.1:c.255G>T
|
ENSP00000472141.1:p.Glu85Asp
|
|
ENST00000597743.5:c.165+231G>T
|
ENSP00000470308.1:n.165+231G>T
|
|
ENST00000597868.5:n.323G>T
|
|
|
ENST00000598871.5:c.147G>T
|
ENSP00000470502.1:p.Glu49Asp
|
|
ENST00000599839.5:c.147G>T
|
ENSP00000471225.1:p.Glu49Asp
|
|
NM_005184.2:c.255G>T
|
NP_005175.2:p.Glu85Asp
|
|
NM_001329921.1:c.147G>T
|
NP_001316850.1:p.Glu49Asp
|
|
NM_001329922.1:c.255G>T
|
NP_001316851.1:p.Glu85Asp
|
|
NM_001329923.1:c.147G>T
|
NP_001316852.1:p.Glu49Asp
|
|
NM_001329924.1:c.147G>T
|
NP_001316853.1:p.Glu49Asp
|
|
NM_001329925.1:c.147G>T
|
NP_001316854.1:p.Glu49Asp
|
|
NM_001329926.1:c.147G>T
|
NP_001316855.1:p.Glu49Asp
|
|
NM_005184.3:c.255G>T
|
NP_005175.2:p.Glu85Asp
|
|
NM_001329924.2:c.147G>T
|
NP_001316853.1:p.Glu49Asp
|
|
NM_001329925.2:c.147G>T
|
NP_001316854.1:p.Glu49Asp
|
|
NM_001329926.2:c.147G>T
|
NP_001316855.1:p.Glu49Asp
|
|
NM_005184.4:c.255G>T
MANE Select
|
NP_005175.2:p.Glu85Asp
|
|