ENST00000340855.11:c.924T>A
MANE Select
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ENSP00000339801.6:p.Asp308Glu
|
|
ENST00000651111.1:c.291T>A
|
ENSP00000498395.1:p.Asp97Glu
|
|
ENST00000340855.10:c.924T>A
|
ENSP00000339801.6:p.Asp308Glu
|
|
ENST00000370441.8:c.924T>A
|
ENSP00000359470.4:p.Asp308Glu
|
|
ENST00000422081.6:c.291T>A
|
ENSP00000477056.1:p.Asp97Glu
|
|
ENST00000441880.1:n.114-3298T>A
|
|
|
ENST00000464251.5:c.850T>A
|
ENSP00000428980.1:n.850T>A
|
|
ENST00000466323.5:c.*115T>A
|
ENSP00000418264.1:n.*115T>A
|
|
ENST00000490775.5:n.709T>A
|
|
|
NM_000202.6:c.924T>A
|
NP_000193.1:p.Asp308Glu
|
|
NM_001166550.2:c.654T>A
|
NP_001160022.1:p.Asp218Glu
|
|
NM_006123.4:c.924T>A
|
NP_006114.1:p.Asp308Glu
|
|
NR_104128.1:n.1271T>A
|
|
|
NM_000202.7:c.924T>A
|
NP_000193.1:p.Asp308Glu
|
|
NM_001166550.3:c.654T>A
|
NP_001160022.1:p.Asp218Glu
|
|
NM_000202.8:c.924T>A
MANE Select
|
NP_000193.1:p.Asp308Glu
|
|
NM_001166550.4:c.654T>A
|
NP_001160022.1:p.Asp218Glu
|
|
NM_006123.5:c.924T>A
|
NP_006114.1:p.Asp308Glu
|
|
NR_104128.2:n.1223T>A
|
|
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