ENST00000257895.10:c.540T>C
MANE Select
|
ENSP00000257895.6:p.Phe180=
|
|
ENST00000257895.9:c.540T>C
|
ENSP00000257895.5:p.Phe180=
|
|
ENST00000257899.3:c.555T>C
|
|
|
ENST00000547072.5:c.249T>C
|
ENSP00000449927.1:p.Phe83=
|
|
ENST00000548082.1:c.540T>C
|
ENSP00000447128.1:p.Phe180=
|
|
ENST00000548123.1:c.300+424T>C
|
|
|
ENST00000548486.1:n.550T>C
|
|
|
ENST00000550412.5:c.*212T>C
|
ENSP00000447650.1:n.*212T>C
|
|
ENST00000550608.1:n.679T>C
|
|
|
ENST00000551946.5:c.*343T>C
|
ENSP00000450201.1:n.*343T>C
|
|
ENST00000553160.1:n.406-277T>C
|
|
|
ENST00000553187.5:n.550T>C
|
|
|
NM_001199771.1:c.540T>C
|
NP_001186700.1:p.Phe180=
|
|
NM_002905.3:c.540T>C
|
NP_002896.2:p.Phe180=
|
|
NR_037658.1:n.599T>C
|
|
|
NM_001199771.2:c.540T>C
|
NP_001186700.1:p.Phe180=
|
|
NM_002905.5:c.540T>C
MANE Select
|
NP_002896.2:p.Phe180=
|
|
NM_001199771.3:c.540T>C
|
NP_001186700.1:p.Phe180=
|
|