ENST00000682276.1:n.1206A>T
|
|
|
ENST00000682892.1:c.1308A>T
|
ENSP00000507214.1:p.Ser436=
|
|
ENST00000682952.1:n.1400A>T
|
|
|
ENST00000684455.1:c.974A>T
|
|
|
ENST00000684642.1:c.1158A>T
|
ENSP00000507355.1:p.Ser386=
|
|
ENST00000303236.9:c.1761A>T
MANE Select
|
ENSP00000307235.3:p.Ser587=
|
|
ENST00000652099.1:c.1955A>T
|
|
|
ENST00000652736.1:n.1637A>T
|
|
|
ENST00000303236.7:c.1761A>T
|
ENSP00000307235.3:p.Ser587=
|
|
ENST00000415570.1:c.1398A>T
|
ENSP00000412076.1:p.Ser466=
|
|
ENST00000419748.5:c.1308A>T
|
ENSP00000408325.1:p.Ser436=
|
|
NM_001313915.1:c.1308A>T
|
NP_001300844.1:p.Ser436=
|
|
NM_004836.5:c.1761A>T
|
NP_004827.4:p.Ser587=
|
|
NM_004836.6:c.1761A>T
|
NP_004827.4:p.Ser587=
|
|
XM_005264649.3:c.1077A>T
|
XP_005264706.1:p.Ser359=
|
|
XR_939749.1:n.1970A>T
|
|
|
XM_017005376.2:c.1077A>T
|
XP_016860865.1:p.Ser359=
|
|
NM_004836.7:c.1761A>T
MANE Select
|
NP_004827.4:p.Ser587=
|
|
NM_001313915.2:c.1308A>T
|
NP_001300844.1:p.Ser436=
|
|