ENST00000388958.8:c.1189T>G
|
ENSP00000373610.3:p.Leu397Val
|
|
ENST00000646100.2:c.1189T>G
MANE Select
|
ENSP00000496564.2:p.Leu397Val
|
|
ENST00000647277.1:c.*3T>G
|
ENSP00000495594.1:n.*3T>G
|
|
ENST00000286149.8:c.1231T>G
|
ENSP00000286149.4:p.Leu411Val
|
|
ENST00000388956.8:c.952T>G
|
ENSP00000373608.4:p.Leu318Val
|
|
ENST00000388957.3:c.217T>G
|
ENSP00000373609.3:p.Leu73Val
|
|
ENST00000388958.7:c.1189T>G
|
ENSP00000373610.3:p.Leu397Val
|
|
ENST00000563871.5:n.409T>G
|
|
|
NM_001161683.1:c.952T>G
|
NP_001155155.1:p.Leu318Val
|
|
NM_144672.3:c.1189T>G
|
NP_653273.3:p.Leu397Val
|
|
NM_170664.2:c.217T>G
|
NP_733764.1:p.Leu73Val
|
|
XM_011545747.1:c.1189T>G
|
XP_011544049.1:p.Leu397Val
|
|
XM_011545748.1:c.58T>G
|
XP_011544050.1:p.Leu20Val
|
|
NM_144672.4:c.1189T>G
MANE Select
|
NP_653273.3:p.Leu397Val
|
|
XM_011545748.2:c.58T>G
|
XP_011544050.2:p.Leu20Val
|
|
XR_002957775.1:n.284T>G
|
|
|
NM_001161683.2:c.952T>G
|
NP_001155155.1:p.Leu318Val
|
|
NM_170664.3:c.217T>G
|
NP_733764.1:p.Leu73Val
|
|