ENST00000333590.6:c.251C>G
MANE Select
|
ENSP00000369820.3:p.Thr84Ser
|
|
ENST00000637296.1:c.-315+194C>G
|
ENSP00000490545.1:n.-315+194C>G
|
|
ENST00000637626.1:c.251C>G
|
ENSP00000489928.1:p.Thr84Ser
|
|
ENST00000638131.1:c.111+140C>G
|
ENSP00000490483.1:n.111+140C>G
|
|
ENST00000333590.5:c.251C>G
|
ENSP00000369820.3:p.Thr84Ser
|
|
ENST00000474662.2:n.142+194C>G
|
|
|
ENST00000482148.6:c.251C>G
|
ENSP00000489528.1:p.Thr84Ser
|
|
ENST00000542278.6:c.251C>G
|
ENSP00000442653.2:p.Thr84Ser
|
|
ENST00000634286.1:c.44C>G
|
ENSP00000489491.1:p.Thr15Ser
|
|
ENST00000634582.1:c.13+3821C>G
|
ENSP00000489540.1:n.13+3821C>G
|
|
ENST00000634640.1:c.-231+194C>G
|
ENSP00000489083.1:n.-231+194C>G
|
|
ENST00000635045.1:n.336C>G
|
|
|
ENST00000635543.1:c.251C>G
|
ENSP00000489205.1:p.Thr84Ser
|
|
ENST00000635598.1:c.251C>G
|
ENSP00000489207.1:p.Thr84Ser
|
|
NM_002641.3:c.251C>G , LRG_160t1:c.251C>G
|
NP_002632.1:p.Thr84Ser
|
|
NM_020473.3:c.13+3821C>G
|
NP_065206.3:n.13+3821C>G
|
|
NR_033835.1:n.367C>G
|
|
|
NR_033836.1:n.173+194C>G
|
|
|
NM_002641.4:c.251C>G
MANE Select
|
NP_002632.1:p.Thr84Ser
|
|