ENST00000393716.8:c.9G>A
MANE Select
|
ENSP00000377319.3:p.Val3=
|
|
ENST00000466380.6:c.9G>A
|
ENSP00000420297.2:p.Val3=
|
|
ENST00000648112.1:c.*32G>A
|
ENSP00000497876.1:n.*32G>A
|
|
ENST00000337940.4:c.126G>A
|
ENSP00000336528.4:p.Val42=
|
|
ENST00000393716.6:c.9G>A
|
ENSP00000377319.2:p.Val3=
|
|
ENST00000466380.5:c.9G>A
|
ENSP00000420297.1:p.Val3=
|
|
ENST00000474090.1:n.297G>A
|
|
|
NM_003889.3:c.9G>A
|
NP_003880.3:p.Val3=
|
|
NM_022002.2:c.126G>A
|
NP_071285.1:p.Val42=
|
|
NM_033013.2:c.9G>A
|
NP_148934.1:p.Val3=
|
|
NM_003889.4:c.9G>A
MANE Select
|
NP_003880.3:p.Val3=
|
|
NM_022002.3:c.126G>A
|
NP_071285.1:p.Val42=
|
|
NM_033013.3:c.9G>A
|
NP_148934.1:p.Val3=
|
|