ENST00000398603.6:c.337-246C>T
|
ENSP00000381604.1:n.337-246C>T
|
|
ENST00000398606.10:c.376C>T
MANE Select
|
ENSP00000381607.3:p.Gln126Ter
|
|
ENST00000646888.1:c.*92C>T
|
ENSP00000494477.1:n.*92C>T
|
|
ENST00000398603.5:c.337-246C>T
|
ENSP00000381604.1:n.337-246C>T
|
|
ENST00000398606.7:c.376C>T
|
ENSP00000381607.3:p.Gln126Ter
|
|
ENST00000467591.1:n.487C>T
|
|
|
ENST00000494593.1:n.1171C>T
|
|
|
ENST00000495996.1:c.40C>T
|
ENSP00000484686.1:p.Gln14Ter
|
|
ENST00000498765.5:c.439C>T
|
|
|
NM_000852.3:c.376C>T , LRG_723t1:c.376C>T
|
NP_000843.1:p.Gln126Ter
|
|
NM_000852.4:c.376C>T
MANE Select
|
NP_000843.1:p.Gln126Ter
|
|