ENST00000478003.2:n.2032A>G
|
|
|
ENST00000682276.1:n.1649A>G
|
|
|
ENST00000682892.1:c.1751A>G
|
ENSP00000507214.1:p.Glu584Gly
|
|
ENST00000682952.1:n.1843A>G
|
|
|
ENST00000684455.1:c.1417A>G
|
|
|
ENST00000684642.1:c.1601A>G
|
ENSP00000507355.1:p.Glu534Gly
|
|
ENST00000684740.1:n.2382A>G
|
|
|
ENST00000303236.9:c.2204A>G
MANE Select
|
ENSP00000307235.3:p.Glu735Gly
|
|
ENST00000652099.1:c.2398A>G
|
|
|
ENST00000652736.1:n.2080A>G
|
|
|
ENST00000303236.7:c.2204A>G
|
ENSP00000307235.3:p.Glu735Gly
|
|
ENST00000415570.1:c.1841A>G
|
ENSP00000412076.1:p.Glu614Gly
|
|
ENST00000419748.5:c.1751A>G
|
ENSP00000408325.1:p.Glu584Gly
|
|
ENST00000470706.1:n.48+82A>G
|
|
|
NM_001313915.1:c.1751A>G
|
NP_001300844.1:p.Glu584Gly
|
|
NM_004836.5:c.2204A>G
|
NP_004827.4:p.Glu735Gly
|
|
NM_004836.6:c.2204A>G
|
NP_004827.4:p.Glu735Gly
|
|
NR_110236.1:n.1416T>C
|
|
|
XM_005264649.3:c.1520A>G
|
XP_005264706.1:p.Glu507Gly
|
|
XR_939749.1:n.2483A>G
|
|
|
XM_017005376.2:c.1520A>G
|
XP_016860865.1:p.Glu507Gly
|
|
NM_004836.7:c.2204A>G
MANE Select
|
NP_004827.4:p.Glu735Gly
|
|
NM_001313915.2:c.1751A>G
|
NP_001300844.1:p.Glu584Gly
|
|