ENST00000340855.11:c.701A>G
MANE Select
|
ENSP00000339801.6:p.Tyr234Cys
|
|
ENST00000651111.1:c.68A>G
|
ENSP00000498395.1:p.Tyr23Cys
|
|
ENST00000340855.10:c.701A>G
|
ENSP00000339801.6:p.Tyr234Cys
|
|
ENST00000370441.8:c.701A>G
|
ENSP00000359470.4:p.Tyr234Cys
|
|
ENST00000422081.6:c.68A>G
|
ENSP00000477056.1:p.Tyr23Cys
|
|
ENST00000441880.1:n.114-11016A>G
|
|
|
ENST00000464251.5:c.627A>G
|
ENSP00000428980.1:n.627A>G
|
|
ENST00000466019.1:n.153A>G
|
|
|
ENST00000466323.5:c.701A>G
|
ENSP00000418264.1:p.Tyr234Cys
|
|
ENST00000490775.5:n.486A>G
|
|
|
NM_000202.6:c.701A>G
|
NP_000193.1:p.Tyr234Cys
|
|
NM_001166550.2:c.431A>G
|
NP_001160022.1:p.Tyr144Cys
|
|
NM_006123.4:c.701A>G
|
NP_006114.1:p.Tyr234Cys
|
|
NR_104128.1:n.918A>G
|
|
|
NM_000202.7:c.701A>G
|
NP_000193.1:p.Tyr234Cys
|
|
NM_001166550.3:c.431A>G
|
NP_001160022.1:p.Tyr144Cys
|
|
NM_000202.8:c.701A>G
MANE Select
|
NP_000193.1:p.Tyr234Cys
|
|
NM_001166550.4:c.431A>G
|
NP_001160022.1:p.Tyr144Cys
|
|
NM_006123.5:c.701A>G
|
NP_006114.1:p.Tyr234Cys
|
|
NR_104128.2:n.870A>G
|
|
|