ENST00000553591.2:c.599C>G
|
ENSP00000452421.2:p.Ala200Gly
|
|
ENST00000556293.6:n.2905C>G
|
|
|
ENST00000556754.2:n.3848C>G
|
|
|
ENST00000557229.6:n.911C>G
|
|
|
ENST00000697613.1:c.482C>G
|
ENSP00000513359.1:p.Ala161Gly
|
|
ENST00000697614.1:c.245C>G
|
ENSP00000513360.1:p.Ala82Gly
|
|
ENST00000697615.1:n.1310C>G
|
|
|
ENST00000361505.10:c.482C>G
MANE Select
|
ENSP00000354532.6:p.Ala161Gly
|
|
ENST00000361505.9:c.482C>G
|
ENSP00000354532.5:p.Ala161Gly
|
|
ENST00000553591.1:c.599C>G
|
ENSP00000452421.1:p.Ala200Gly
|
|
ENST00000554056.5:n.790C>G
|
|
|
ENST00000556754.1:n.1699C>G
|
|
|
ENST00000557229.5:n.911C>G
|
|
|
NM_000270.3:c.482C>G , LRG_91t1:c.482C>G
|
NP_000261.2:p.Ala161Gly
|
|
NM_000270.4:c.482C>G
MANE Select
|
NP_000261.2:p.Ala161Gly
|
|