ENST00000478003.2:n.2246A>T
|
|
|
ENST00000682276.1:n.1863A>T
|
|
|
ENST00000682892.1:c.1965A>T
|
ENSP00000507214.1:p.Ile655=
|
|
ENST00000682952.1:n.2057A>T
|
|
|
ENST00000684455.1:c.1631A>T
|
|
|
ENST00000684642.1:c.1815A>T
|
ENSP00000507355.1:p.Ile605=
|
|
ENST00000684740.1:n.2596A>T
|
|
|
ENST00000303236.9:c.2418A>T
MANE Select
|
ENSP00000307235.3:p.Ile806=
|
|
ENST00000652099.1:c.2612A>T
|
|
|
ENST00000652736.1:n.2294A>T
|
|
|
ENST00000303236.7:c.2418A>T
|
ENSP00000307235.3:p.Ile806=
|
|
ENST00000415570.1:c.2055A>T
|
ENSP00000412076.1:p.Ile685=
|
|
ENST00000419748.5:c.1965A>T
|
ENSP00000408325.1:p.Ile655=
|
|
ENST00000470706.1:n.61A>T
|
|
|
NM_001313915.1:c.1965A>T
|
NP_001300844.1:p.Ile655=
|
|
NM_004836.5:c.2418A>T
|
NP_004827.4:p.Ile806=
|
|
NM_004836.6:c.2418A>T
|
NP_004827.4:p.Ile806=
|
|
NR_110236.1:n.1202T>A
|
|
|
XM_005264649.3:c.1734A>T
|
XP_005264706.1:p.Ile578=
|
|
XM_017005376.2:c.1734A>T
|
XP_016860865.1:p.Ile578=
|
|
NM_004836.7:c.2418A>T
MANE Select
|
NP_004827.4:p.Ile806=
|
|
NM_001313915.2:c.1965A>T
|
NP_001300844.1:p.Ile655=
|
|