ENST00000398603.6:c.337-244A>G
|
ENSP00000381604.1:n.337-244A>G
|
|
ENST00000398606.10:c.378A>G
MANE Select
|
ENSP00000381607.3:p.Gln126=
|
|
ENST00000646888.1:c.*94A>G
|
ENSP00000494477.1:n.*94A>G
|
|
ENST00000398603.5:c.337-244A>G
|
ENSP00000381604.1:n.337-244A>G
|
|
ENST00000398606.7:c.378A>G
|
ENSP00000381607.3:p.Gln126=
|
|
ENST00000467591.1:n.489A>G
|
|
|
ENST00000494593.1:n.1173A>G
|
|
|
ENST00000495996.1:c.42A>G
|
ENSP00000484686.1:p.Gln14=
|
|
ENST00000498765.5:c.441A>G
|
|
|
NM_000852.3:c.378A>G , LRG_723t1:c.378A>G
|
NP_000843.1:p.Gln126=
|
|
NM_000852.4:c.378A>G
MANE Select
|
NP_000843.1:p.Gln126=
|
|