ENST00000388958.8:c.1190T>A
|
ENSP00000373610.3:p.Leu397Ter
|
|
ENST00000646100.2:c.1190T>A
MANE Select
|
ENSP00000496564.2:p.Leu397Ter
|
|
ENST00000647277.1:c.*4T>A
|
ENSP00000495594.1:n.*4T>A
|
|
ENST00000286149.8:c.1232T>A
|
ENSP00000286149.4:p.Leu411Ter
|
|
ENST00000388956.8:c.953T>A
|
ENSP00000373608.4:p.Leu318Ter
|
|
ENST00000388957.3:c.218T>A
|
ENSP00000373609.3:p.Leu73Ter
|
|
ENST00000388958.7:c.1190T>A
|
ENSP00000373610.3:p.Leu397Ter
|
|
ENST00000563871.5:n.410T>A
|
|
|
NM_001161683.1:c.953T>A
|
NP_001155155.1:p.Leu318Ter
|
|
NM_144672.3:c.1190T>A
|
NP_653273.3:p.Leu397Ter
|
|
NM_170664.2:c.218T>A
|
NP_733764.1:p.Leu73Ter
|
|
XM_011545747.1:c.1190T>A
|
XP_011544049.1:p.Leu397Ter
|
|
XM_011545748.1:c.59T>A
|
XP_011544050.1:p.Leu20Ter
|
|
NM_144672.4:c.1190T>A
MANE Select
|
NP_653273.3:p.Leu397Ter
|
|
XM_011545748.2:c.59T>A
|
XP_011544050.2:p.Leu20Ter
|
|
XR_002957775.1:n.285T>A
|
|
|
NM_001161683.2:c.953T>A
|
NP_001155155.1:p.Leu318Ter
|
|
NM_170664.3:c.218T>A
|
NP_733764.1:p.Leu73Ter
|
|