ENST00000456935.7:c.412G>A
MANE Select
|
ENSP00000395473.2:p.Val138Ile
|
|
ENST00000221363.8:c.412G>A
|
ENSP00000221363.4:p.Val138Ile
|
|
ENST00000456935.6:c.412G>A
|
ENSP00000395473.2:p.Val138Ile
|
|
ENST00000466794.5:n.394G>A
|
|
|
ENST00000486847.2:c.309G>A
|
ENSP00000470174.1:p.Lys103=
|
|
ENST00000596512.5:n.350G>A
|
|
|
ENST00000597961.1:c.403G>A
|
ENSP00000472710.1:p.Val135Ile
|
|
ENST00000598876.1:c.439G>A
|
ENSP00000470533.1:p.Val147Ile
|
|
ENST00000600281.1:n.453G>A
|
|
|
NM_000528.3:c.412G>A
|
NP_000519.2:p.Val138Ile
|
|
NM_001173498.1:c.412G>A
|
NP_001166969.1:p.Val138Ile
|
|
XM_005259913.1:c.412G>A
|
XP_005259970.1:p.Val138Ile
|
|
XM_005259913.2:c.412G>A
|
XP_005259970.1:p.Val138Ile
|
|
XM_024451518.1:c.-607G>A
|
XP_024307286.1:n.-607G>A
|
|
NM_000528.4:c.412G>A
MANE Select
|
NP_000519.2:p.Val138Ile
|
|
NM_001173498.2:c.412G>A
|
NP_001166969.1:p.Val138Ile
|
|