ENST00000478003.2:n.2045A>T
|
|
|
ENST00000682276.1:n.1662A>T
|
|
|
ENST00000682892.1:c.1764A>T
|
ENSP00000507214.1:p.Ser588=
|
|
ENST00000682952.1:n.1856A>T
|
|
|
ENST00000684455.1:c.1430A>T
|
|
|
ENST00000684642.1:c.1614A>T
|
ENSP00000507355.1:p.Ser538=
|
|
ENST00000684740.1:n.2395A>T
|
|
|
ENST00000303236.9:c.2217A>T
MANE Select
|
ENSP00000307235.3:p.Ser739=
|
|
ENST00000652099.1:c.2411A>T
|
|
|
ENST00000652736.1:n.2093A>T
|
|
|
ENST00000303236.7:c.2217A>T
|
ENSP00000307235.3:p.Ser739=
|
|
ENST00000415570.1:c.1854A>T
|
ENSP00000412076.1:p.Ser618=
|
|
ENST00000419748.5:c.1764A>T
|
ENSP00000408325.1:p.Ser588=
|
|
ENST00000470706.1:n.48+95A>T
|
|
|
NM_001313915.1:c.1764A>T
|
NP_001300844.1:p.Ser588=
|
|
NM_004836.5:c.2217A>T
|
NP_004827.4:p.Ser739=
|
|
NM_004836.6:c.2217A>T
|
NP_004827.4:p.Ser739=
|
|
NR_110236.1:n.1403T>A
|
|
|
XM_005264649.3:c.1533A>T
|
XP_005264706.1:p.Ser511=
|
|
XR_939749.1:n.2496A>T
|
|
|
XM_017005376.2:c.1533A>T
|
XP_016860865.1:p.Ser511=
|
|
NM_004836.7:c.2217A>T
MANE Select
|
NP_004827.4:p.Ser739=
|
|
NM_001313915.2:c.1764A>T
|
NP_001300844.1:p.Ser588=
|
|