ENST00000374490.8:c.722C>G
MANE Select
|
ENSP00000363614.3:p.Ala241Gly
|
|
ENST00000235958.4:c.292C>G
|
|
|
ENST00000374487.6:c.*763C>G
|
ENSP00000363611.2:n.*763C>G
|
|
ENST00000374490.7:c.722C>G
|
ENSP00000363614.3:p.Ala241Gly
|
|
ENST00000436439.6:c.509C>G
|
ENSP00000389281.2:p.Ala170Gly
|
|
ENST00000496907.1:n.357C>G
|
|
|
ENST00000509389.5:n.413C>G
|
|
|
NM_000191.2:c.722C>G
|
NP_000182.2:p.Ala241Gly
|
|
NM_001166059.1:c.509C>G
|
NP_001159531.1:p.Ala170Gly
|
|
NM_000191.3:c.722C>G
MANE Select
|
NP_000182.2:p.Ala241Gly
|
|
NM_001166059.2:c.509C>G
|
NP_001159531.1:p.Ala170Gly
|
|