ENST00000255078.8:c.1506G>A
MANE Select
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ENSP00000255078.4:p.Glu502=
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ENST00000674955.1:c.*223G>A
|
ENSP00000502463.1:n.*223G>A
|
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ENST00000675118.1:c.994G>A
|
|
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ENST00000675205.1:n.183+401G>A
|
|
|
ENST00000675615.1:c.1506G>A
|
ENSP00000502413.1:p.Glu502=
|
|
ENST00000675648.1:n.881G>A
|
|
|
ENST00000675997.1:n.113-582G>A
|
|
|
ENST00000676173.1:n.2251G>A
|
|
|
ENST00000676228.1:c.*829G>A
|
ENSP00000502375.1:n.*829G>A
|
|
ENST00000255078.7:c.1506G>A
|
ENSP00000255078.3:p.Glu502=
|
|
ENST00000537458.5:n.623G>A
|
|
|
ENST00000539064.5:n.1265G>A
|
|
|
ENST00000541229.5:n.201G>A
|
|
|
ENST00000543739.5:n.623G>A
|
|
|
NM_002180.2:c.1506G>A , LRG_250t1:c.1506G>A
|
NP_002171.2:p.Glu502=
|
|
XM_005273974.2:c.495G>A
|
XP_005274031.1:p.Glu165=
|
|
XM_005273975.2:c.378G>A
|
XP_005274032.1:p.Glu126=
|
|
XM_011544994.1:c.273G>A
|
XP_011543296.1:p.Glu91=
|
|
XR_949903.1:n.1608G>A
|
|
|
XM_005273975.3:c.378G>A
|
XP_005274032.1:p.Glu126=
|
|
XM_017017669.2:c.495G>A
|
XP_016873158.1:p.Glu165=
|
|
XM_017017670.2:c.495G>A
|
XP_016873159.1:p.Glu165=
|
|
XM_017017671.2:c.1506G>A
|
XP_016873160.1:p.Glu502=
|
|
XR_949903.3:n.1604G>A
|
|
|
NM_002180.3:c.1506G>A
MANE Select
|
NP_002171.2:p.Glu502=
|
|