ENST00000481739.2:c.355G>T
MANE Select
|
ENSP00000419692.1:p.Val119Phe
|
|
ENST00000672570.1:c.274G>T
|
ENSP00000500402.1:p.Val92Phe
|
|
ENST00000356384.4:n.765G>T
|
|
|
ENST00000481739.1:c.355G>T
|
ENSP00000419692.1:p.Val119Phe
|
|
NM_001291920.1:c.274G>T
|
NP_001278849.1:p.Val92Phe
|
|
NM_001291921.1:c.64G>T
|
NP_001278850.1:p.Val22Phe
|
|
NM_002957.5:c.355G>T
|
NP_002948.1:p.Val119Phe
|
|
NM_002957.6:c.355G>T
MANE Select
|
NP_002948.1:p.Val119Phe
|
|
NM_001291921.2:c.64G>T
|
NP_001278850.1:p.Val22Phe
|
|
NM_001291920.2:c.274G>T
|
NP_001278849.1:p.Val92Phe
|
|