ENST00000398603.6:c.337-234T>G
|
ENSP00000381604.1:n.337-234T>G
|
|
ENST00000398606.10:c.388T>G
MANE Select
|
ENSP00000381607.3:p.Phe130Val
|
|
ENST00000646888.1:c.*104T>G
|
ENSP00000494477.1:n.*104T>G
|
|
ENST00000398603.5:c.337-234T>G
|
ENSP00000381604.1:n.337-234T>G
|
|
ENST00000398606.7:c.388T>G
|
ENSP00000381607.3:p.Phe130Val
|
|
ENST00000467591.1:n.499T>G
|
|
|
ENST00000494593.1:n.1183T>G
|
|
|
ENST00000495996.1:c.52T>G
|
ENSP00000484686.1:p.Phe18Val
|
|
ENST00000498765.5:c.451T>G
|
|
|
NM_000852.3:c.388T>G , LRG_723t1:c.388T>G
|
NP_000843.1:p.Phe130Val
|
|
NM_000852.4:c.388T>G
MANE Select
|
NP_000843.1:p.Phe130Val
|
|