ENST00000481739.2:c.430G>T
MANE Select
|
ENSP00000419692.1:p.Gly144Cys
|
|
ENST00000672570.1:c.349G>T
|
ENSP00000500402.1:p.Gly117Cys
|
|
ENST00000356384.4:n.840G>T
|
|
|
ENST00000481739.1:c.430G>T
|
ENSP00000419692.1:p.Gly144Cys
|
|
NM_001291920.1:c.349G>T
|
NP_001278849.1:p.Gly117Cys
|
|
NM_001291921.1:c.139G>T
|
NP_001278850.1:p.Gly47Cys
|
|
NM_002957.5:c.430G>T
|
NP_002948.1:p.Gly144Cys
|
|
NM_002957.6:c.430G>T
MANE Select
|
NP_002948.1:p.Gly144Cys
|
|
NM_001291921.2:c.139G>T
|
NP_001278850.1:p.Gly47Cys
|
|
NM_001291920.2:c.349G>T
|
NP_001278849.1:p.Gly117Cys
|
|