ENST00000478003.2:n.2111C>T
|
|
|
ENST00000682276.1:n.1728C>T
|
|
|
ENST00000682892.1:c.1830C>T
|
ENSP00000507214.1:p.Leu610=
|
|
ENST00000682952.1:n.1922C>T
|
|
|
ENST00000684455.1:c.1496C>T
|
|
|
ENST00000684642.1:c.1680C>T
|
ENSP00000507355.1:p.Leu560=
|
|
ENST00000684740.1:n.2461C>T
|
|
|
ENST00000303236.9:c.2283C>T
MANE Select
|
ENSP00000307235.3:p.Leu761=
|
|
ENST00000652099.1:c.2477C>T
|
|
|
ENST00000652736.1:n.2159C>T
|
|
|
ENST00000303236.7:c.2283C>T
|
ENSP00000307235.3:p.Leu761=
|
|
ENST00000415570.1:c.1920C>T
|
ENSP00000412076.1:p.Leu640=
|
|
ENST00000419748.5:c.1830C>T
|
ENSP00000408325.1:p.Leu610=
|
|
ENST00000470706.1:n.49-123C>T
|
|
|
NM_001313915.1:c.1830C>T
|
NP_001300844.1:p.Leu610=
|
|
NM_004836.5:c.2283C>T
|
NP_004827.4:p.Leu761=
|
|
NM_004836.6:c.2283C>T
|
NP_004827.4:p.Leu761=
|
|
NR_110236.1:n.1337G>A
|
|
|
XM_005264649.3:c.1599C>T
|
XP_005264706.1:p.Leu533=
|
|
XM_017005376.2:c.1599C>T
|
XP_016860865.1:p.Leu533=
|
|
NM_004836.7:c.2283C>T
MANE Select
|
NP_004827.4:p.Leu761=
|
|
NM_001313915.2:c.1830C>T
|
NP_001300844.1:p.Leu610=
|
|