ENST00000281928.9:c.5148G>A
MANE Select
|
ENSP00000281928.3:p.Glu1716=
|
|
ENST00000549786.2:c.4576G>A
|
|
|
ENST00000648379.1:n.3516G>A
|
|
|
ENST00000648737.1:n.4912G>A
|
|
|
ENST00000648825.1:n.1888G>A
|
|
|
ENST00000648916.1:n.3159G>A
|
|
|
ENST00000649146.1:n.2391G>A
|
|
|
ENST00000649607.1:c.3332G>A
|
|
|
ENST00000649775.1:c.1637G>A
|
|
|
ENST00000650226.1:c.5148G>A
|
ENSP00000496981.1:p.Glu1716=
|
|
ENST00000281928.7:c.5148G>A
|
ENSP00000281928.3:p.Glu1716=
|
|
ENST00000549786.1:c.512G>A
|
|
|
ENST00000552340.1:c.180G>A
|
ENSP00000449876.1:p.Glu60=
|
|
NM_015335.4:c.5148G>A
|
NP_056150.1:p.Glu1716=
|
|
XM_011538080.1:c.5148G>A
|
XP_011536382.1:p.Glu1716=
|
|
XM_011538081.1:c.5145G>A
|
XP_011536383.1:p.Glu1715=
|
|
XM_011538082.1:c.5118G>A
|
XP_011536384.1:p.Glu1706=
|
|
XM_011538080.2:c.5148G>A
|
XP_011536382.1:p.Glu1716=
|
|
XM_011538081.2:c.5145G>A
|
XP_011536383.1:p.Glu1715=
|
|
XM_011538082.2:c.5118G>A
|
XP_011536384.1:p.Glu1706=
|
|
XM_017019090.1:c.5145G>A
|
XP_016874579.1:p.Glu1715=
|
|
NM_015335.5:c.5148G>A
MANE Select
|
NP_056150.1:p.Glu1716=
|
|