ENST00000398603.6:c.343T>A
|
ENSP00000381604.1:p.Phe115Ile
|
|
ENST00000398606.10:c.451T>A
MANE Select
|
ENSP00000381607.3:p.Phe151Ile
|
|
ENST00000646888.1:c.*167T>A
|
ENSP00000494477.1:n.*167T>A
|
|
ENST00000398603.5:c.343T>A
|
ENSP00000381604.1:p.Phe115Ile
|
|
ENST00000398606.7:c.451T>A
|
ENSP00000381607.3:p.Phe151Ile
|
|
ENST00000467591.1:n.562T>A
|
|
|
ENST00000494593.1:n.1423T>A
|
|
|
ENST00000495996.1:c.177T>A
|
ENSP00000484686.1:p.Pro59=
|
|
ENST00000498765.5:c.514T>A
|
|
|
NM_000852.3:c.451T>A , LRG_723t1:c.451T>A
|
NP_000843.1:p.Phe151Ile
|
|
NM_000852.4:c.451T>A
MANE Select
|
NP_000843.1:p.Phe151Ile
|
|