ENST00000374490.8:c.710C>G
MANE Select
|
ENSP00000363614.3:p.Thr237Ser
|
|
ENST00000235958.4:c.280C>G
|
|
|
ENST00000374487.6:c.*751C>G
|
ENSP00000363611.2:n.*751C>G
|
|
ENST00000374490.7:c.710C>G
|
ENSP00000363614.3:p.Thr237Ser
|
|
ENST00000436439.6:c.497C>G
|
ENSP00000389281.2:p.Thr166Ser
|
|
ENST00000496907.1:n.345C>G
|
|
|
ENST00000509389.5:n.401C>G
|
|
|
NM_000191.2:c.710C>G
|
NP_000182.2:p.Thr237Ser
|
|
NM_001166059.1:c.497C>G
|
NP_001159531.1:p.Thr166Ser
|
|
NM_000191.3:c.710C>G
MANE Select
|
NP_000182.2:p.Thr237Ser
|
|
NM_001166059.2:c.497C>G
|
NP_001159531.1:p.Thr166Ser
|
|