ENST00000398603.6:c.368T>A
|
ENSP00000381604.1:p.Leu123Ter
|
|
ENST00000398606.10:c.476T>A
MANE Select
|
ENSP00000381607.3:p.Leu159Ter
|
|
ENST00000646888.1:c.*192T>A
|
ENSP00000494477.1:n.*192T>A
|
|
ENST00000398603.5:c.368T>A
|
ENSP00000381604.1:p.Leu123Ter
|
|
ENST00000398606.7:c.476T>A
|
ENSP00000381607.3:p.Leu159Ter
|
|
ENST00000467591.1:n.587T>A
|
|
|
ENST00000494593.1:n.1448T>A
|
|
|
ENST00000495996.1:c.202T>A
|
ENSP00000484686.1:p.Cys68Ser
|
|
ENST00000498765.5:c.539T>A
|
|
|
NM_000852.3:c.476T>A , LRG_723t1:c.476T>A
|
NP_000843.1:p.Leu159Ter
|
|
NM_000852.4:c.476T>A
MANE Select
|
NP_000843.1:p.Leu159Ter
|
|