ENST00000478003.2:n.2198T>C
|
|
|
ENST00000682276.1:n.1815T>C
|
|
|
ENST00000682892.1:c.1917T>C
|
ENSP00000507214.1:p.Ser639=
|
|
ENST00000682952.1:n.2009T>C
|
|
|
ENST00000684455.1:c.1583T>C
|
|
|
ENST00000684642.1:c.1767T>C
|
ENSP00000507355.1:p.Ser589=
|
|
ENST00000684740.1:n.2548T>C
|
|
|
ENST00000303236.9:c.2370T>C
MANE Select
|
ENSP00000307235.3:p.Ser790=
|
|
ENST00000652099.1:c.2564T>C
|
|
|
ENST00000652736.1:n.2246T>C
|
|
|
ENST00000303236.7:c.2370T>C
|
ENSP00000307235.3:p.Ser790=
|
|
ENST00000415570.1:c.2007T>C
|
ENSP00000412076.1:p.Ser669=
|
|
ENST00000419748.5:c.1917T>C
|
ENSP00000408325.1:p.Ser639=
|
|
ENST00000470706.1:n.49-36T>C
|
|
|
NM_001313915.1:c.1917T>C
|
NP_001300844.1:p.Ser639=
|
|
NM_004836.5:c.2370T>C
|
NP_004827.4:p.Ser790=
|
|
NM_004836.6:c.2370T>C
|
NP_004827.4:p.Ser790=
|
|
NR_110236.1:n.1250A>G
|
|
|
XM_005264649.3:c.1686T>C
|
XP_005264706.1:p.Ser562=
|
|
XM_017005376.2:c.1686T>C
|
XP_016860865.1:p.Ser562=
|
|
NM_004836.7:c.2370T>C
MANE Select
|
NP_004827.4:p.Ser790=
|
|
NM_001313915.2:c.1917T>C
|
NP_001300844.1:p.Ser639=
|
|