ENST00000255078.8:c.1454G>A
MANE Select
|
ENSP00000255078.4:p.Gly485Asp
|
|
ENST00000674955.1:c.*171G>A
|
ENSP00000502463.1:n.*171G>A
|
|
ENST00000675118.1:c.942G>A
|
|
|
ENST00000675205.1:n.183+349G>A
|
|
|
ENST00000675615.1:c.1454G>A
|
ENSP00000502413.1:p.Gly485Asp
|
|
ENST00000675648.1:n.829G>A
|
|
|
ENST00000675997.1:n.113-634G>A
|
|
|
ENST00000676173.1:n.2199G>A
|
|
|
ENST00000676228.1:c.*777G>A
|
ENSP00000502375.1:n.*777G>A
|
|
ENST00000255078.7:c.1454G>A
|
ENSP00000255078.3:p.Gly485Asp
|
|
ENST00000537458.5:n.571G>A
|
|
|
ENST00000539064.5:n.1213G>A
|
|
|
ENST00000541229.5:n.149G>A
|
|
|
ENST00000543739.5:n.571G>A
|
|
|
NM_002180.2:c.1454G>A , LRG_250t1:c.1454G>A
|
NP_002171.2:p.Gly485Asp
|
|
XM_005273974.2:c.443G>A
|
XP_005274031.1:p.Gly148Asp
|
|
XM_005273975.2:c.326G>A
|
XP_005274032.1:p.Gly109Asp
|
|
XM_011544994.1:c.221G>A
|
XP_011543296.1:p.Gly74Asp
|
|
XR_949903.1:n.1556G>A
|
|
|
XM_005273975.3:c.326G>A
|
XP_005274032.1:p.Gly109Asp
|
|
XM_017017669.2:c.443G>A
|
XP_016873158.1:p.Gly148Asp
|
|
XM_017017670.2:c.443G>A
|
XP_016873159.1:p.Gly148Asp
|
|
XM_017017671.2:c.1454G>A
|
XP_016873160.1:p.Gly485Asp
|
|
XR_949903.3:n.1552G>A
|
|
|
NM_002180.3:c.1454G>A
MANE Select
|
NP_002171.2:p.Gly485Asp
|
|