ENST00000478003.2:n.2184G>A
|
|
|
ENST00000682276.1:n.1801G>A
|
|
|
ENST00000682892.1:c.1903G>A
|
ENSP00000507214.1:p.Glu635Lys
|
|
ENST00000682952.1:n.1995G>A
|
|
|
ENST00000684455.1:c.1569G>A
|
|
|
ENST00000684642.1:c.1753G>A
|
ENSP00000507355.1:p.Glu585Lys
|
|
ENST00000684740.1:n.2534G>A
|
|
|
ENST00000303236.9:c.2356G>A
MANE Select
|
ENSP00000307235.3:p.Glu786Lys
|
|
ENST00000652099.1:c.2550G>A
|
|
|
ENST00000652736.1:n.2232G>A
|
|
|
ENST00000303236.7:c.2356G>A
|
ENSP00000307235.3:p.Glu786Lys
|
|
ENST00000415570.1:c.1993G>A
|
ENSP00000412076.1:p.Glu665Lys
|
|
ENST00000419748.5:c.1903G>A
|
ENSP00000408325.1:p.Glu635Lys
|
|
ENST00000470706.1:n.49-50G>A
|
|
|
NM_001313915.1:c.1903G>A
|
NP_001300844.1:p.Glu635Lys
|
|
NM_004836.5:c.2356G>A
|
NP_004827.4:p.Glu786Lys
|
|
NM_004836.6:c.2356G>A
|
NP_004827.4:p.Glu786Lys
|
|
NR_110236.1:n.1264C>T
|
|
|
XM_005264649.3:c.1672G>A
|
XP_005264706.1:p.Glu558Lys
|
|
XM_017005376.2:c.1672G>A
|
XP_016860865.1:p.Glu558Lys
|
|
NM_004836.7:c.2356G>A
MANE Select
|
NP_004827.4:p.Glu786Lys
|
|
NM_001313915.2:c.1903G>A
|
NP_001300844.1:p.Glu635Lys
|
|