ENST00000478003.2:n.1947G>T
|
|
|
ENST00000682276.1:n.1564G>T
|
|
|
ENST00000682892.1:c.1666G>T
|
ENSP00000507214.1:p.Glu556Ter
|
|
ENST00000682952.1:n.1758G>T
|
|
|
ENST00000684455.1:c.1332G>T
|
|
|
ENST00000684642.1:c.1516G>T
|
ENSP00000507355.1:p.Glu506Ter
|
|
ENST00000684740.1:n.2297G>T
|
|
|
ENST00000303236.9:c.2119G>T
MANE Select
|
ENSP00000307235.3:p.Glu707Ter
|
|
ENST00000652099.1:c.2313G>T
|
|
|
ENST00000652736.1:n.1995G>T
|
|
|
ENST00000303236.7:c.2119G>T
|
ENSP00000307235.3:p.Glu707Ter
|
|
ENST00000415570.1:c.1756G>T
|
ENSP00000412076.1:p.Glu586Ter
|
|
ENST00000419748.5:c.1666G>T
|
ENSP00000408325.1:p.Glu556Ter
|
|
ENST00000470706.1:n.45G>T
|
|
|
NM_001313915.1:c.1666G>T
|
NP_001300844.1:p.Glu556Ter
|
|
NM_004836.5:c.2119G>T
|
NP_004827.4:p.Glu707Ter
|
|
NM_004836.6:c.2119G>T
|
NP_004827.4:p.Glu707Ter
|
|
NR_110236.1:n.1501C>A
|
|
|
XM_005264649.3:c.1435G>T
|
XP_005264706.1:p.Glu479Ter
|
|
XR_939749.1:n.2398G>T
|
|
|
XM_017005376.2:c.1435G>T
|
XP_016860865.1:p.Glu479Ter
|
|
NM_004836.7:c.2119G>T
MANE Select
|
NP_004827.4:p.Glu707Ter
|
|
NM_001313915.2:c.1666G>T
|
NP_001300844.1:p.Glu556Ter
|
|