ENST00000340855.11:c.407T>G
MANE Select
|
ENSP00000339801.6:p.Val136Gly
|
|
ENST00000651111.1:c.-215-2286T>G
|
ENSP00000498395.1:n.-215-2286T>G
|
|
ENST00000340855.10:c.407T>G
|
ENSP00000339801.6:p.Val136Gly
|
|
ENST00000370441.8:c.407T>G
|
ENSP00000359470.4:p.Val136Gly
|
|
ENST00000422081.6:c.-215-2286T>G
|
ENSP00000477056.1:n.-215-2286T>G
|
|
ENST00000427113.2:n.770-1100T>G
|
|
|
ENST00000428056.6:c.407T>G
|
ENSP00000390241.2:p.Val136Gly
|
|
ENST00000441880.1:n.114-16225T>G
|
|
|
ENST00000464251.5:c.230T>G
|
ENSP00000428980.1:p.Val77Gly
|
|
ENST00000466323.5:c.407T>G
|
ENSP00000418264.1:p.Val136Gly
|
|
ENST00000490775.5:n.66T>G
|
|
|
ENST00000523759.5:n.533-2286T>G
|
|
|
NM_000202.6:c.407T>G
|
NP_000193.1:p.Val136Gly
|
|
NM_001166550.2:c.137T>G
|
NP_001160022.1:p.Val46Gly
|
|
NM_006123.4:c.407T>G
|
NP_006114.1:p.Val136Gly
|
|
NR_104128.1:n.624T>G
|
|
|
NM_000202.7:c.407T>G
|
NP_000193.1:p.Val136Gly
|
|
NM_001166550.3:c.137T>G
|
NP_001160022.1:p.Val46Gly
|
|
NM_000202.8:c.407T>G
MANE Select
|
NP_000193.1:p.Val136Gly
|
|
NM_001166550.4:c.137T>G
|
NP_001160022.1:p.Val46Gly
|
|
NM_006123.5:c.407T>G
|
NP_006114.1:p.Val136Gly
|
|
NR_104128.2:n.576T>G
|
|
|