ENST00000389805.9:c.387T>G
MANE Select
|
ENSP00000374455.4:p.Asp129Glu
|
|
ENST00000360718.5:c.135T>G
|
ENSP00000353944.5:p.Asp45Glu
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ENST00000389805.8:c.387T>G
|
ENSP00000374455.4:p.Asp129Glu
|
|
ENST00000422245.5:c.135T>G
|
ENSP00000394534.1:p.Asp45Glu
|
|
ENST00000464493.5:n.282T>G
|
|
|
ENST00000466342.1:n.86T>G
|
|
|
ENST00000481335.5:n.537T>G
|
|
|
ENST00000485412.1:n.379T>G
|
|
|
ENST00000504627.1:c.456T>G
|
ENSP00000425957.1:p.Asp152Glu
|
|
ENST00000508284.5:c.*109T>G
|
ENSP00000424195.1:n.*109T>G
|
|
ENST00000510187.5:c.387T>G
|
ENSP00000424477.1:p.Asp129Glu
|
|
ENST00000514093.5:c.135T>G
|
ENSP00000427308.1:p.Asp45Glu
|
|
NM_001142298.1:c.135T>G
|
NP_001135770.1:p.Asp45Glu
|
|
NM_001142299.1:c.135T>G
|
NP_001135771.1:p.Asp45Glu
|
|
NM_003900.4:c.387T>G
|
NP_003891.1:p.Asp129Glu
|
|
XM_017010010.1:c.135T>G
|
XP_016865499.1:p.Asp45Glu
|
|
NM_003900.5:c.387T>G
MANE Select
|
NP_003891.1:p.Asp129Glu
|
|
NM_001142298.2:c.135T>G
|
NP_001135770.1:p.Asp45Glu
|
|
NM_001142299.2:c.135T>G
|
NP_001135771.1:p.Asp45Glu
|
|