ENST00000553591.2:c.592T>G
|
ENSP00000452421.2:p.Phe198Val
|
|
ENST00000556293.6:n.2898T>G
|
|
|
ENST00000556754.2:n.3841T>G
|
|
|
ENST00000557229.6:n.904T>G
|
|
|
ENST00000697613.1:c.475T>G
|
ENSP00000513359.1:p.Phe159Val
|
|
ENST00000697614.1:c.238T>G
|
ENSP00000513360.1:p.Phe80Val
|
|
ENST00000697615.1:n.1303T>G
|
|
|
ENST00000361505.10:c.475T>G
MANE Select
|
ENSP00000354532.6:p.Phe159Val
|
|
ENST00000361505.9:c.475T>G
|
ENSP00000354532.5:p.Phe159Val
|
|
ENST00000553591.1:c.592T>G
|
ENSP00000452421.1:p.Phe198Val
|
|
ENST00000554056.5:n.783T>G
|
|
|
ENST00000556754.1:n.1692T>G
|
|
|
ENST00000557229.5:n.904T>G
|
|
|
NM_000270.3:c.475T>G , LRG_91t1:c.475T>G
|
NP_000261.2:p.Phe159Val
|
|
NM_000270.4:c.475T>G
MANE Select
|
NP_000261.2:p.Phe159Val
|
|