ENST00000682565.1:c.11726C>T
|
ENSP00000507671.1:p.Thr3909Ile
|
|
ENST00000682801.1:c.11167-756C>T
|
ENSP00000507862.1:n.11167-756C>T
|
|
ENST00000682859.1:c.11726C>T
|
ENSP00000508222.1:p.Thr3909Ile
|
|
ENST00000683791.1:c.4812C>T
|
|
|
ENST00000684460.1:c.9007C>T
|
|
|
ENST00000684548.1:c.11726C>T
|
ENSP00000507421.1:p.Thr3909Ile
|
|
ENST00000684590.1:c.6173C>T
|
ENSP00000507376.1:p.Thr2058Ile
|
|
ENST00000684656.1:c.9191C>T
|
|
|
ENST00000613296.6:c.12107C>T
MANE Select
|
ENSP00000482968.1:p.Thr4036Ile
|
|
ENST00000651057.1:c.2261C>T
|
ENSP00000498504.1:p.Thr754Ile
|
|
ENST00000651434.1:c.3463C>T
|
|
|
ENST00000651750.1:c.1260+548C>T
|
|
|
ENST00000652487.1:c.3278C>T
|
|
|
ENST00000464408.3:n.282C>T
|
|
|
ENST00000484298.5:c.11981C>T
|
ENSP00000478155.1:p.Thr3994Ile
|
|
ENST00000613296.4:c.12107C>T
|
ENSP00000482968.1:p.Thr4036Ile
|
|
ENST00000620466.4:n.5910C>T
|
|
|
NM_015120.4:c.12110C>T , LRG_741t1:c.12110C>T
|
NP_055935.4:p.Thr4037Ile
|
|
NM_001378454.1:c.12107C>T
MANE Select
|
NP_001365383.1:p.Thr4036Ile
|
|