ENST00000478003.2:n.1867C>G
|
|
|
ENST00000682276.1:n.1484C>G
|
|
|
ENST00000682892.1:c.1586C>G
|
ENSP00000507214.1:p.Thr529Arg
|
|
ENST00000682952.1:n.1678C>G
|
|
|
ENST00000684455.1:c.1252C>G
|
|
|
ENST00000684642.1:c.1436C>G
|
ENSP00000507355.1:p.Thr479Arg
|
|
ENST00000684740.1:n.2217C>G
|
|
|
ENST00000303236.9:c.2039C>G
MANE Select
|
ENSP00000307235.3:p.Thr680Arg
|
|
ENST00000652099.1:c.2233C>G
|
|
|
ENST00000652736.1:n.1915C>G
|
|
|
ENST00000303236.7:c.2039C>G
|
ENSP00000307235.3:p.Thr680Arg
|
|
ENST00000415570.1:c.1676C>G
|
ENSP00000412076.1:p.Thr559Arg
|
|
ENST00000419748.5:c.1586C>G
|
ENSP00000408325.1:p.Thr529Arg
|
|
ENST00000478003.1:n.605C>G
|
|
|
NM_001313915.1:c.1586C>G
|
NP_001300844.1:p.Thr529Arg
|
|
NM_004836.5:c.2039C>G
|
NP_004827.4:p.Thr680Arg
|
|
NM_004836.6:c.2039C>G
|
NP_004827.4:p.Thr680Arg
|
|
NR_110236.1:n.1581G>C
|
|
|
XM_005264649.3:c.1355C>G
|
XP_005264706.1:p.Thr452Arg
|
|
XR_939749.1:n.2318C>G
|
|
|
XM_017005376.2:c.1355C>G
|
XP_016860865.1:p.Thr452Arg
|
|
NM_004836.7:c.2039C>G
MANE Select
|
NP_004827.4:p.Thr680Arg
|
|
NM_001313915.2:c.1586C>G
|
NP_001300844.1:p.Thr529Arg
|
|