ENST00000398603.6:c.337-244A>T
|
ENSP00000381604.1:n.337-244A>T
|
|
ENST00000398606.10:c.378A>T
MANE Select
|
ENSP00000381607.3:p.Gln126His
|
|
ENST00000646888.1:c.*94A>T
|
ENSP00000494477.1:n.*94A>T
|
|
ENST00000398603.5:c.337-244A>T
|
ENSP00000381604.1:n.337-244A>T
|
|
ENST00000398606.7:c.378A>T
|
ENSP00000381607.3:p.Gln126His
|
|
ENST00000467591.1:n.489A>T
|
|
|
ENST00000494593.1:n.1173A>T
|
|
|
ENST00000495996.1:c.42A>T
|
ENSP00000484686.1:p.Gln14His
|
|
ENST00000498765.5:c.441A>T
|
|
|
NM_000852.3:c.378A>T , LRG_723t1:c.378A>T
|
NP_000843.1:p.Gln126His
|
|
NM_000852.4:c.378A>T
MANE Select
|
NP_000843.1:p.Gln126His
|
|