ENST00000463045.3:c.367C>T
|
ENSP00000481376.2:p.Leu123=
|
|
ENST00000491274.6:c.496C>T
|
ENSP00000480482.2:p.Leu166=
|
|
ENST00000375499.8:c.538C>T
MANE Select
|
ENSP00000364649.3:p.Leu180=
|
|
ENST00000375499.7:c.538C>T
|
ENSP00000364649.3:p.Leu180=
|
|
ENST00000463045.2:c.367C>T
|
ENSP00000481376.1:p.Leu123=
|
|
ENST00000475506.1:n.455C>T
|
|
|
ENST00000485515.5:n.472C>T
|
|
|
ENST00000491274.5:c.496C>T
|
ENSP00000480482.1:p.Leu166=
|
|
NM_003000.2:c.538C>T , LRG_316t1:c.538C>T
|
NP_002991.2:p.Leu180=
|
|
NM_003000.3:c.538C>T
MANE Select
|
NP_002991.2:p.Leu180=
|
|