ENST00000452035.7:n.2329T>G
|
|
|
ENST00000483004.2:c.1626T>G
|
ENSP00000419887.2:p.Thr542=
|
|
ENST00000698628.1:c.1625-213T>G
|
ENSP00000513848.1:n.1625-213T>G
|
|
ENST00000698629.1:n.2114T>G
|
|
|
ENST00000698630.1:n.2558T>G
|
|
|
ENST00000698631.1:n.2559T>G
|
|
|
ENST00000698632.1:n.3448T>G
|
|
|
ENST00000698633.1:n.3338T>G
|
|
|
ENST00000425368.7:c.1842T>G
MANE Select
|
ENSP00000416561.2:p.Thr614=
|
|
ENST00000425368.6:c.1842T>G
|
ENSP00000416561.2:p.Thr614=
|
|
ENST00000456570.5:c.3348T>G
|
ENSP00000410815.1:p.Thr1116=
|
|
ENST00000467360.1:n.968T>G
|
|
|
ENST00000477310.1:c.2895T>G
|
ENSP00000418996.1:p.Thr965=
|
|
ENST00000482312.1:n.58T>G
|
|
|
ENST00000483004.1:c.464T>G
|
|
|
NM_001710.5:c.1842T>G , LRG_136t1:c.1842T>G
|
NP_001701.2:p.Thr614=
|
|
NM_001710.6:c.1842T>G
MANE Select
|
NP_001701.2:p.Thr614=
|
|