ENST00000293778.12:c.719A>T
MANE Select
|
ENSP00000293778.7:p.Asp240Val
|
|
ENST00000574412.6:c.719A>T
|
ENSP00000459592.2:p.Asp240Val
|
|
ENST00000293778.10:c.776A>T
|
ENSP00000293778.6:p.Asp259Val
|
|
ENST00000574412.5:c.776A>T
|
ENSP00000459592.1:p.Asp259Val
|
|
ENST00000575168.1:n.550A>T
|
|
|
ENST00000576153.5:n.510A>T
|
|
|
NM_001100812.1:c.776A>T
|
NP_001094282.1:p.Asp259Val
|
|
NM_022059.3:c.776A>T
|
NP_071342.2:p.Asp259Val
|
|
NM_022059.4:c.776A>T
|
NP_071342.2:p.Asp259Val
|
|
NM_001100812.2:c.719A>T
|
NP_001094282.2:p.Asp240Val
|
|
NM_001386809.1:c.719A>T
MANE Select
|
NP_001373738.1:p.Asp240Val
|
|