ENST00000398603.6:c.354C>T
|
ENSP00000381604.1:p.Tyr118=
|
|
ENST00000398606.10:c.462C>T
MANE Select
|
ENSP00000381607.3:p.Tyr154=
|
|
ENST00000646888.1:c.*178C>T
|
ENSP00000494477.1:n.*178C>T
|
|
ENST00000398603.5:c.354C>T
|
ENSP00000381604.1:p.Tyr118=
|
|
ENST00000398606.7:c.462C>T
|
ENSP00000381607.3:p.Tyr154=
|
|
ENST00000467591.1:n.573C>T
|
|
|
ENST00000494593.1:n.1434C>T
|
|
|
ENST00000495996.1:c.188C>T
|
ENSP00000484686.1:p.Thr63Ile
|
|
ENST00000498765.5:c.525C>T
|
|
|
NM_000852.3:c.462C>T , LRG_723t1:c.462C>T
|
NP_000843.1:p.Tyr154=
|
|
NM_000852.4:c.462C>T
MANE Select
|
NP_000843.1:p.Tyr154=
|
|