ENST00000232607.7:c.412G>A
MANE Select
|
ENSP00000232607.2:p.Val138Ile
|
|
ENST00000232607.6:c.412G>A
|
ENSP00000232607.2:p.Val138Ile
|
|
ENST00000460034.5:c.*156G>A
|
ENSP00000420409.1:n.*156G>A
|
|
ENST00000462091.5:c.*84G>A
|
ENSP00000417893.1:n.*84G>A
|
|
ENST00000467167.5:c.*310G>A
|
ENSP00000419618.1:n.*310G>A
|
|
ENST00000474588.5:c.311-246G>A
|
ENSP00000420348.1:n.311-246G>A
|
|
ENST00000479719.5:c.412G>A
|
ENSP00000420754.1:p.Val138Ile
|
|
ENST00000497791.5:c.*84G>A
|
ENSP00000419121.1:n.*84G>A
|
|
ENST00000498715.1:n.130G>A
|
|
|
NM_000373.3:c.412G>A
|
NP_000364.1:p.Val138Ile
|
|
NR_033434.1:n.364G>A
|
|
|
NR_033437.1:n.617G>A
|
|
|
XR_001740253.2:n.442G>A
|
|
|
NM_000373.4:c.412G>A
MANE Select
|
NP_000364.1:p.Val138Ile
|
|
NR_033434.2:n.278G>A
|
|
|
NR_033437.2:n.531G>A
|
|
|