ENST00000426304.6:c.349T>A
|
ENSP00000394896.2:p.Phe117Ile
|
|
ENST00000457600.3:c.349T>A
|
ENSP00000407201.2:p.Phe117Ile
|
|
ENST00000698174.1:c.349T>A
|
ENSP00000513594.1:p.Phe117Ile
|
|
ENST00000698175.1:c.*96T>A
|
ENSP00000513595.1:n.*96T>A
|
|
ENST00000698176.1:n.421T>A
|
|
|
ENST00000698202.1:c.349T>A
|
ENSP00000513605.1:p.Phe117Ile
|
|
ENST00000698203.1:c.349T>A
|
ENSP00000513606.1:p.Phe117Ile
|
|
ENST00000356853.10:c.349T>A
MANE Select
|
ENSP00000349313.5:p.Phe117Ile
|
|
ENST00000318673.6:c.*1471T>A
|
ENSP00000320919.3:n.*1471T>A
|
|
ENST00000356853.9:c.349T>A
|
ENSP00000349313.5:p.Phe117Ile
|
|
ENST00000409720.5:c.349T>A
|
ENSP00000387290.1:p.Phe117Ile
|
|
ENST00000418099.5:c.349T>A
|
ENSP00000408966.1:p.Phe117Ile
|
|
ENST00000426304.5:c.109T>A
|
ENSP00000394896.1:p.Phe37Ile
|
|
ENST00000450447.1:c.*36T>A
|
ENSP00000408421.1:n.*36T>A
|
|
ENST00000457600.2:c.349T>A
|
ENSP00000407201.1:p.Phe117Ile
|
|
ENST00000498327.5:n.2537T>A
|
|
|
NM_024782.2:c.349T>A , LRG_90t1:c.349T>A
|
NP_079058.1:p.Phe117Ile
|
|
NM_001377498.1:c.349T>A
|
NP_001364427.1:p.Phe117Ile
|
|
NM_001377499.1:c.349T>A
|
NP_001364428.1:p.Phe117Ile
|
|
NM_024782.3:c.349T>A
MANE Select
|
NP_079058.1:p.Phe117Ile
|
|
NR_165304.1:n.445T>A
|
|
|