ENST00000299106.9:c.387T>G
MANE Select
|
ENSP00000299106.4:p.Ile129Met
|
|
ENST00000299106.8:c.387T>G
|
ENSP00000299106.4:p.Ile129Met
|
|
ENST00000441717.3:c.257-421T>G
|
ENSP00000395742.3:n.257-421T>G
|
|
ENST00000524969.5:n.451T>G
|
|
|
ENST00000531302.5:n.386T>G
|
|
|
ENST00000532165.1:n.417T>G
|
|
|
ENST00000532252.5:c.*377T>G
|
ENSP00000432455.1:n.*377T>G
|
|
ENST00000534549.5:c.207T>G
|
ENSP00000433206.1:p.Ile69Met
|
|
NM_001205329.1:c.257-421T>G
|
NP_001192258.1:n.257-421T>G
|
|
NM_032801.4:c.387T>G
|
NP_116190.3:p.Ile129Met
|
|
NM_032801.5:c.387T>G
MANE Select
|
NP_116190.3:p.Ile129Met
|
|
NM_001205329.2:c.257-421T>G
|
NP_001192258.1:n.257-421T>G
|
|