ENST00000257895.10:c.529G>T
MANE Select
|
ENSP00000257895.6:p.Val177Phe
|
|
ENST00000257895.9:c.529G>T
|
ENSP00000257895.5:p.Val177Phe
|
|
ENST00000257899.3:c.544G>T
|
|
|
ENST00000547072.5:c.238G>T
|
ENSP00000449927.1:p.Val80Phe
|
|
ENST00000548082.1:c.529G>T
|
ENSP00000447128.1:p.Val177Phe
|
|
ENST00000548123.1:c.300+413G>T
|
|
|
ENST00000548486.1:n.539G>T
|
|
|
ENST00000550412.5:c.*201G>T
|
ENSP00000447650.1:n.*201G>T
|
|
ENST00000550608.1:n.668G>T
|
|
|
ENST00000551946.5:c.*332G>T
|
ENSP00000450201.1:n.*332G>T
|
|
ENST00000553160.1:n.406-288G>T
|
|
|
ENST00000553187.5:n.539G>T
|
|
|
NM_001199771.1:c.529G>T
|
NP_001186700.1:p.Val177Phe
|
|
NM_002905.3:c.529G>T
|
NP_002896.2:p.Val177Phe
|
|
NR_037658.1:n.588G>T
|
|
|
NM_001199771.2:c.529G>T
|
NP_001186700.1:p.Val177Phe
|
|
NM_002905.5:c.529G>T
MANE Select
|
NP_002896.2:p.Val177Phe
|
|
NM_001199771.3:c.529G>T
|
NP_001186700.1:p.Val177Phe
|
|