ENST00000293778.12:c.728T>A
MANE Select
|
ENSP00000293778.7:p.Val243Asp
|
|
ENST00000574412.6:c.728T>A
|
ENSP00000459592.2:p.Val243Asp
|
|
ENST00000293778.10:c.785T>A
|
ENSP00000293778.6:p.Val262Asp
|
|
ENST00000574412.5:c.785T>A
|
ENSP00000459592.1:p.Val262Asp
|
|
ENST00000575168.1:n.559T>A
|
|
|
ENST00000576153.5:n.519T>A
|
|
|
NM_001100812.1:c.785T>A
|
NP_001094282.1:p.Val262Asp
|
|
NM_022059.3:c.785T>A
|
NP_071342.2:p.Val262Asp
|
|
NM_022059.4:c.785T>A
|
NP_071342.2:p.Val262Asp
|
|
NM_001100812.2:c.728T>A
|
NP_001094282.2:p.Val243Asp
|
|
NM_001386809.1:c.728T>A
MANE Select
|
NP_001373738.1:p.Val243Asp
|
|