ENST00000592793.6:n.3170C>T
|
|
|
ENST00000682020.1:c.440C>T
|
ENSP00000508075.1:p.Thr147Ile
|
|
ENST00000682206.1:c.*126C>T
|
ENSP00000508285.1:n.*126C>T
|
|
ENST00000682314.1:n.1082C>T
|
|
|
ENST00000682327.1:c.506C>T
|
ENSP00000507058.1:p.Thr169Ile
|
|
ENST00000682349.1:n.3176C>T
|
|
|
ENST00000682703.1:n.4002C>T
|
|
|
ENST00000682797.1:c.*126C>T
|
ENSP00000507582.1:n.*126C>T
|
|
ENST00000682985.1:c.545C>T
|
ENSP00000507598.1:p.Thr182Ile
|
|
ENST00000683433.1:c.290C>T
|
ENSP00000507463.1:p.Thr97Ile
|
|
ENST00000683685.1:n.1908C>T
|
|
|
ENST00000683710.1:c.*1001C>T
|
ENSP00000506785.1:n.*1001C>T
|
|
ENST00000683739.1:c.701C>T
|
ENSP00000507002.1:p.Thr234Ile
|
|
ENST00000683772.1:n.1078C>T
|
|
|
ENST00000684008.1:c.972C>T
|
ENSP00000507962.1:n.972C>T
|
|
ENST00000684190.1:c.995C>T
|
ENSP00000507554.1:p.Thr332Ile
|
|
ENST00000684335.1:c.961+1211C>T
|
ENSP00000508112.1:n.961+1211C>T
|
|
ENST00000262374.10:c.1034C>T
MANE Select
|
ENSP00000262374.5:p.Thr345Ile
|
|
ENST00000650085.1:n.1858C>T
|
|
|
ENST00000262374.9:c.1034C>T
|
ENSP00000262374.4:p.Thr345Ile
|
|
ENST00000544428.1:c.701C>T
|
ENSP00000440019.1:p.Thr234Ile
|
|
ENST00000588623.5:c.701C>T
|
ENSP00000468118.1:p.Thr234Ile
|
|
ENST00000591822.5:c.*935C>T
|
ENSP00000467865.1:n.*935C>T
|
|
NM_019109.4:c.1034C>T
|
NP_061982.3:p.Thr345Ile
|
|
XM_011522565.1:c.701C>T
|
XP_011520867.1:p.Thr234Ile
|
|
NM_001330504.1:c.701C>T
|
NP_001317433.1:p.Thr234Ile
|
|
XM_017023457.2:c.995C>T
|
XP_016878946.1:p.Thr332Ile
|
|
XM_017023458.1:c.701C>T
|
XP_016878947.1:p.Thr234Ile
|
|
XR_932882.3:n.1063C>T
|
|
|
NM_019109.5:c.1034C>T
MANE Select
|
NP_061982.3:p.Thr345Ile
|
|
NM_001330504.2:c.701C>T
|
NP_001317433.1:p.Thr234Ile
|
|