ENST00000340855.11:c.590C>G
MANE Select
|
ENSP00000339801.6:p.Pro197Arg
|
|
ENST00000651111.1:c.-44C>G
|
ENSP00000498395.1:n.-44C>G
|
|
ENST00000340855.10:c.590C>G
|
ENSP00000339801.6:p.Pro197Arg
|
|
ENST00000370441.8:c.590C>G
|
ENSP00000359470.4:p.Pro197Arg
|
|
ENST00000422081.6:c.-44C>G
|
ENSP00000477056.1:n.-44C>G
|
|
ENST00000441880.1:n.114-11127C>G
|
|
|
ENST00000464251.5:c.516C>G
|
ENSP00000428980.1:n.516C>G
|
|
ENST00000466019.1:n.42C>G
|
|
|
ENST00000466323.5:c.590C>G
|
ENSP00000418264.1:p.Pro197Arg
|
|
ENST00000490775.5:n.375C>G
|
|
|
ENST00000523759.5:n.704C>G
|
|
|
NM_000202.6:c.590C>G
|
NP_000193.1:p.Pro197Arg
|
|
NM_001166550.2:c.320C>G
|
NP_001160022.1:p.Pro107Arg
|
|
NM_006123.4:c.590C>G
|
NP_006114.1:p.Pro197Arg
|
|
NR_104128.1:n.807C>G
|
|
|
NM_000202.7:c.590C>G
|
NP_000193.1:p.Pro197Arg
|
|
NM_001166550.3:c.320C>G
|
NP_001160022.1:p.Pro107Arg
|
|
NM_000202.8:c.590C>G
MANE Select
|
NP_000193.1:p.Pro197Arg
|
|
NM_001166550.4:c.320C>G
|
NP_001160022.1:p.Pro107Arg
|
|
NM_006123.5:c.590C>G
|
NP_006114.1:p.Pro197Arg
|
|
NR_104128.2:n.759C>G
|
|
|