ENST00000301761.7:c.477G>T
MANE Select
|
ENSP00000301761.3:p.Glu159Asp
|
|
ENST00000301761.6:c.477G>T
|
ENSP00000301761.2:p.Glu159Asp
|
|
ENST00000536670.5:n.396+7934G>T
|
|
|
ENST00000537782.5:c.*123G>T
|
ENSP00000469951.1:n.*123G>T
|
|
ENST00000538594.5:c.370+7934G>T
|
ENSP00000440939.1:n.370+7934G>T
|
|
ENST00000541135.5:c.377+7927G>T
|
ENSP00000443130.1:n.377+7927G>T
|
|
ENST00000542074.1:c.*56G>T
|
ENSP00000469670.1:n.*56G>T
|
|
ENST00000542794.5:c.*479G>T
|
ENSP00000439983.1:n.*479G>T
|
|
ENST00000543044.2:c.441G>T
|
ENSP00000440219.1:p.Glu147Asp
|
|
ENST00000543265.1:c.*100G>T
|
ENSP00000443660.1:n.*100G>T
|
|
ENST00000544025.5:n.465+7934G>T
|
|
|
ENST00000544801.5:c.370+7934G>T
|
ENSP00000442581.1:n.370+7934G>T
|
|
ENST00000544880.1:n.374+7934G>T
|
|
|
NM_017841.2:c.477G>T , LRG_519t1:c.477G>T
|
NP_060311.1:p.Glu159Asp
|
|
NM_017841.4:c.477G>T
MANE Select
|
NP_060311.1:p.Glu159Asp
|
|