ENST00000330062.8:c.382C>T
MANE Select
|
ENSP00000331897.4:p.Leu128=
|
|
ENST00000330062.7:c.382C>T
|
ENSP00000331897.3:p.Leu128=
|
|
ENST00000540499.2:c.226C>T
|
ENSP00000446147.2:p.Leu76=
|
|
ENST00000559482.5:c.208-237C>T
|
ENSP00000453016.1:n.208-237C>T
|
|
ENST00000560061.1:c.*7C>T
|
ENSP00000453254.1:n.*7C>T
|
|
NM_001289910.1:c.226C>T , LRG_611t1:c.226C>T
|
NP_001276839.1:p.Leu76=
|
|
NM_001290114.1:c.-9C>T
|
NP_001277043.1:n.-9C>T
|
|
NM_002168.3:c.382C>T , LRG_611t2:c.382C>T
|
NP_002159.2:p.Leu128=
|
|
NM_001290114.2:c.-9C>T
|
NP_001277043.1:n.-9C>T
|
|
NM_002168.4:c.382C>T
MANE Select
|
NP_002159.2:p.Leu128=
|
|