ENST00000398603.6:c.337-226C>A
|
ENSP00000381604.1:n.337-226C>A
|
|
ENST00000398606.10:c.396C>A
MANE Select
|
ENSP00000381607.3:p.Thr132=
|
|
ENST00000646888.1:c.*112C>A
|
ENSP00000494477.1:n.*112C>A
|
|
ENST00000398603.5:c.337-226C>A
|
ENSP00000381604.1:n.337-226C>A
|
|
ENST00000398606.7:c.396C>A
|
ENSP00000381607.3:p.Thr132=
|
|
ENST00000467591.1:n.507C>A
|
|
|
ENST00000494593.1:n.1191C>A
|
|
|
ENST00000495996.1:c.60C>A
|
ENSP00000484686.1:p.Thr20=
|
|
ENST00000498765.5:c.459C>A
|
|
|
NM_000852.3:c.396C>A , LRG_723t1:c.396C>A
|
NP_000843.1:p.Thr132=
|
|
NM_000852.4:c.396C>A
MANE Select
|
NP_000843.1:p.Thr132=
|
|