ENST00000281928.9:c.5070G>A
MANE Select
|
ENSP00000281928.3:p.Glu1690=
|
|
ENST00000549786.2:c.4498G>A
|
|
|
ENST00000648379.1:n.3438G>A
|
|
|
ENST00000648737.1:n.4834G>A
|
|
|
ENST00000648825.1:n.1810G>A
|
|
|
ENST00000648916.1:n.3081G>A
|
|
|
ENST00000649146.1:n.2313G>A
|
|
|
ENST00000649607.1:c.3254G>A
|
|
|
ENST00000649775.1:c.1559G>A
|
|
|
ENST00000650226.1:c.5070G>A
|
ENSP00000496981.1:p.Glu1690=
|
|
ENST00000281928.7:c.5070G>A
|
ENSP00000281928.3:p.Glu1690=
|
|
ENST00000549786.1:c.434G>A
|
|
|
ENST00000552340.1:c.102G>A
|
ENSP00000449876.1:p.Glu34=
|
|
NM_015335.4:c.5070G>A
|
NP_056150.1:p.Glu1690=
|
|
XM_011538080.1:c.5070G>A
|
XP_011536382.1:p.Glu1690=
|
|
XM_011538081.1:c.5067G>A
|
XP_011536383.1:p.Glu1689=
|
|
XM_011538082.1:c.5040G>A
|
XP_011536384.1:p.Glu1680=
|
|
XM_011538080.2:c.5070G>A
|
XP_011536382.1:p.Glu1690=
|
|
XM_011538081.2:c.5067G>A
|
XP_011536383.1:p.Glu1689=
|
|
XM_011538082.2:c.5040G>A
|
XP_011536384.1:p.Glu1680=
|
|
XM_017019090.1:c.5067G>A
|
XP_016874579.1:p.Glu1689=
|
|
NM_015335.5:c.5070G>A
MANE Select
|
NP_056150.1:p.Glu1690=
|
|