ENST00000255078.8:c.987A>G
MANE Select
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ENSP00000255078.4:p.Glu329=
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ENST00000674745.1:c.75A>G
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ENSP00000502738.1:p.Glu25=
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ENST00000674775.1:n.75A>G
|
|
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ENST00000674955.1:c.987A>G
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ENSP00000502463.1:p.Glu329=
|
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ENST00000675118.1:c.475A>G
|
|
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ENST00000675119.1:c.414A>G
|
ENSP00000501861.1:n.414A>G
|
|
ENST00000675305.1:c.307A>G
|
ENSP00000502365.1:n.307A>G
|
|
ENST00000675464.1:c.270A>G
|
ENSP00000502650.1:p.Glu90=
|
|
ENST00000675493.1:n.75A>G
|
|
|
ENST00000675615.1:c.987A>G
|
ENSP00000502413.1:p.Glu329=
|
|
ENST00000675648.1:n.362A>G
|
|
|
ENST00000675683.1:c.374A>G
|
|
|
ENST00000675684.1:c.75A>G
|
ENSP00000502192.1:p.Glu25=
|
|
ENST00000676173.1:n.1031A>G
|
|
|
ENST00000676228.1:c.*310A>G
|
ENSP00000502375.1:n.*310A>G
|
|
ENST00000255078.7:c.987A>G
|
ENSP00000255078.3:p.Glu329=
|
|
NM_002180.2:c.987A>G , LRG_250t1:c.987A>G
|
NP_002171.2:p.Glu329=
|
|
XM_005273974.2:c.-25A>G
|
XP_005274031.1:n.-25A>G
|
|
XM_005273976.1:c.987A>G
|
XP_005274033.1:p.Glu329=
|
|
XR_247198.1:n.1089A>G
|
|
|
XR_949903.1:n.1089A>G
|
|
|
XM_005273976.2:c.987A>G
|
XP_005274033.1:p.Glu329=
|
|
XM_017017669.2:c.-25A>G
|
XP_016873158.1:n.-25A>G
|
|
XM_017017670.2:c.-25A>G
|
XP_016873159.1:n.-25A>G
|
|
XM_017017671.2:c.987A>G
|
XP_016873160.1:p.Glu329=
|
|
XR_949903.3:n.1085A>G
|
|
|
NM_002180.3:c.987A>G
MANE Select
|
NP_002171.2:p.Glu329=
|
|