ENST00000340855.11:c.272T>G
MANE Select
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ENSP00000339801.6:p.Phe91Cys
|
|
ENST00000651111.1:c.-215-2421T>G
|
ENSP00000498395.1:n.-215-2421T>G
|
|
ENST00000340855.10:c.272T>G
|
ENSP00000339801.6:p.Phe91Cys
|
|
ENST00000370441.8:c.272T>G
|
ENSP00000359470.4:p.Phe91Cys
|
|
ENST00000422081.6:c.-215-2421T>G
|
ENSP00000477056.1:n.-215-2421T>G
|
|
ENST00000427113.2:n.770-1235T>G
|
|
|
ENST00000428056.6:c.272T>G
|
ENSP00000390241.2:p.Phe91Cys
|
|
ENST00000441880.1:n.114-16360T>G
|
|
|
ENST00000464251.5:c.95T>G
|
ENSP00000428980.1:p.Phe32Cys
|
|
ENST00000466323.5:c.272T>G
|
ENSP00000418264.1:p.Phe91Cys
|
|
ENST00000523759.5:n.533-2421T>G
|
|
|
NM_000202.6:c.272T>G
|
NP_000193.1:p.Phe91Cys
|
|
NM_001166550.2:c.15-13T>G
|
NP_001160022.1:n.15-13T>G
|
|
NM_006123.4:c.272T>G
|
NP_006114.1:p.Phe91Cys
|
|
NR_104128.1:n.489T>G
|
|
|
NM_000202.7:c.272T>G
|
NP_000193.1:p.Phe91Cys
|
|
NM_001166550.3:c.15-13T>G
|
NP_001160022.1:n.15-13T>G
|
|
NM_000202.8:c.272T>G
MANE Select
|
NP_000193.1:p.Phe91Cys
|
|
NM_001166550.4:c.15-13T>G
|
NP_001160022.1:n.15-13T>G
|
|
NM_006123.5:c.272T>G
|
NP_006114.1:p.Phe91Cys
|
|
NR_104128.2:n.441T>G
|
|
|