ENST00000398603.6:c.337-266A>T
|
ENSP00000381604.1:n.337-266A>T
|
|
ENST00000398606.10:c.356A>T
MANE Select
|
ENSP00000381607.3:p.Tyr119Phe
|
|
ENST00000646888.1:c.*72A>T
|
ENSP00000494477.1:n.*72A>T
|
|
ENST00000398603.5:c.337-266A>T
|
ENSP00000381604.1:n.337-266A>T
|
|
ENST00000398606.7:c.356A>T
|
ENSP00000381607.3:p.Tyr119Phe
|
|
ENST00000467591.1:n.467A>T
|
|
|
ENST00000494593.1:n.1151A>T
|
|
|
ENST00000495996.1:c.20A>T
|
ENSP00000484686.1:p.Tyr7Phe
|
|
ENST00000498765.5:c.419A>T
|
|
|
NM_000852.3:c.356A>T , LRG_723t1:c.356A>T
|
NP_000843.1:p.Tyr119Phe
|
|
NM_000852.4:c.356A>T
MANE Select
|
NP_000843.1:p.Tyr119Phe
|
|