ENST00000396043.4:c.*533T>G
|
ENSP00000379358.4:n.*533T>G
|
|
ENST00000374690.9:c.2185T>G
MANE Select
|
ENSP00000363822.3:p.Leu729Val
|
|
ENST00000396043.3:c.812T>G
|
ENSP00000379358.3:n.812T>G
|
|
ENST00000396044.8:c.2173+5800T>G
|
ENSP00000379359.3:n.2173+5800T>G
|
|
ENST00000612452.5:c.2185T>G
|
ENSP00000484033.2:p.Leu729Val
|
|
ENST00000374690.7:c.2185T>G
|
ENSP00000363822.3:p.Leu729Val
|
|
ENST00000396043.2:c.589T>G
|
ENSP00000379358.2:p.Leu197Val
|
|
ENST00000396044.7:c.2173+5800T>G
|
ENSP00000379359.3:n.2173+5800T>G
|
|
ENST00000612452.4:c.1615T>G
|
ENSP00000484033.1:p.Leu539Val
|
|
NM_000044.3:c.2185T>G
|
NP_000035.2:p.Leu729Val
|
|
NM_001011645.2:c.589T>G
|
NP_001011645.1:p.Leu197Val
|
|
NM_000044.4:c.2185T>G
|
NP_000035.2:p.Leu729Val
|
|
NM_001011645.3:c.589T>G
|
NP_001011645.1:p.Leu197Val
|
|
NM_000044.6:c.2185T>G
MANE Select
|
NP_000035.2:p.Leu729Val
|
|