ENST00000374490.8:c.735C>A
MANE Select
|
ENSP00000363614.3:p.Thr245=
|
|
ENST00000235958.4:c.305C>A
|
|
|
ENST00000374487.6:c.*776C>A
|
ENSP00000363611.2:n.*776C>A
|
|
ENST00000374490.7:c.735C>A
|
ENSP00000363614.3:p.Thr245=
|
|
ENST00000436439.6:c.522C>A
|
ENSP00000389281.2:p.Thr174=
|
|
ENST00000496907.1:n.370C>A
|
|
|
ENST00000509389.5:n.426C>A
|
|
|
NM_000191.2:c.735C>A
|
NP_000182.2:p.Thr245=
|
|
NM_001166059.1:c.522C>A
|
NP_001159531.1:p.Thr174=
|
|
NM_000191.3:c.735C>A
MANE Select
|
NP_000182.2:p.Thr245=
|
|
NM_001166059.2:c.522C>A
|
NP_001159531.1:p.Thr174=
|
|