ENST00000478003.2:n.2023G=
|
|
|
ENST00000682276.1:n.1640G=
|
|
|
ENST00000682892.1:c.1742G=
|
ENSP00000507214.1:p.Ser581=
|
|
ENST00000682952.1:n.1834G=
|
|
|
ENST00000684455.1:c.1408G=
|
|
|
ENST00000684642.1:c.1592G=
|
ENSP00000507355.1:p.Ser531=
|
|
ENST00000684740.1:n.2373G=
|
|
|
ENST00000303236.9:c.2195G=
MANE Select
|
ENSP00000307235.3:p.Ser732=
|
|
ENST00000652099.1:c.2389G=
|
|
|
ENST00000652736.1:n.2071G=
|
|
|
ENST00000303236.7:c.2195G=
|
ENSP00000307235.3:p.Ser732=
|
|
ENST00000415570.1:c.1832G=
|
ENSP00000412076.1:p.Ser611=
|
|
ENST00000419748.5:c.1742G=
|
ENSP00000408325.1:p.Ser581=
|
|
ENST00000470706.1:n.48+73G=
|
|
|
NM_001313915.1:c.1742G=
|
NP_001300844.1:p.Ser581=
|
|
NM_004836.5:c.2195G=
|
NP_004827.4:p.Ser732=
|
|
NM_004836.6:c.2195G=
|
NP_004827.4:p.Ser732=
|
|
NR_110236.1:n.1425C=
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|
|
XM_005264649.3:c.1511G=
|
XP_005264706.1:p.Ser504=
|
|
XR_939749.1:n.2474G=
|
|
|
XM_017005376.2:c.1511G=
|
XP_016860865.1:p.Ser504=
|
|
NM_004836.7:c.2195G=
MANE Select
|
NP_004827.4:p.Ser732=
|
|
NM_001313915.2:c.1742G=
|
NP_001300844.1:p.Ser581=
|
|