ENST00000691183.1:c.*354C>G
|
ENSP00000509954.1:n.*354C>G
|
|
ENST00000378842.8:c.766C>G
MANE Select
|
ENSP00000368119.4:p.Leu256Val
|
|
ENST00000378842.7:c.766C>G
|
ENSP00000368119.3:p.Leu256Val
|
|
ENST00000450095.6:c.439C>G
|
ENSP00000401956.2:p.Leu147Val
|
|
ENST00000473506.6:c.*354C>G
|
ENSP00000432839.2:n.*354C>G
|
|
ENST00000489643.6:n.846C>G
|
|
|
ENST00000554085.5:c.*510C>G
|
ENSP00000450419.1:n.*510C>G
|
|
ENST00000554550.5:c.*386C>G
|
ENSP00000451435.1:n.*386C>G
|
|
ENST00000554638.5:n.1238C>G
|
|
|
ENST00000555020.5:n.1227C>G
|
|
|
ENST00000555086.5:n.770C>G
|
|
|
ENST00000555754.1:n.111C>G
|
|
|
ENST00000556244.1:c.753C>G
|
|
|
ENST00000556278.1:c.432+384C>G
|
ENSP00000451792.1:n.432+384C>G
|
|
ENST00000557706.5:n.1328C>G
|
|
|
NM_000155.3:c.766C>G
|
NP_000146.2:p.Leu256Val
|
|
NM_001258332.1:c.439C>G
|
NP_001245261.1:p.Leu147Val
|
|
NM_000155.4:c.766C>G
MANE Select
|
NP_000146.2:p.Leu256Val
|
|
NM_001258332.2:c.439C>G
|
NP_001245261.1:p.Leu147Val
|
|