ENST00000255078.8:c.890G>A
MANE Select
|
ENSP00000255078.4:p.Arg297Lys
|
|
ENST00000539224.2:c.1019G>A
|
|
|
ENST00000674955.1:c.890G>A
|
ENSP00000502463.1:p.Arg297Lys
|
|
ENST00000675118.1:c.237G>A
|
|
|
ENST00000675119.1:c.179G>A
|
ENSP00000501861.1:p.Arg60Lys
|
|
ENST00000675305.1:c.179G>A
|
ENSP00000502365.1:p.Arg60Lys
|
|
ENST00000675464.1:c.179G>A
|
ENSP00000502650.1:p.Arg60Lys
|
|
ENST00000675615.1:c.890G>A
|
ENSP00000502413.1:p.Arg297Lys
|
|
ENST00000675683.1:c.277G>A
|
|
|
ENST00000676173.1:n.934G>A
|
|
|
ENST00000676228.1:c.*213G>A
|
ENSP00000502375.1:n.*213G>A
|
|
ENST00000676239.1:n.204G>A
|
|
|
ENST00000255078.7:c.890G>A
|
ENSP00000255078.3:p.Arg297Lys
|
|
NM_002180.2:c.890G>A , LRG_250t1:c.890G>A
|
NP_002171.2:p.Arg297Lys
|
|
XM_005273974.2:c.-122G>A
|
XP_005274031.1:n.-122G>A
|
|
XM_005273976.1:c.890G>A
|
XP_005274033.1:p.Arg297Lys
|
|
XR_247198.1:n.992G>A
|
|
|
XR_949903.1:n.992G>A
|
|
|
XM_005273976.2:c.890G>A
|
XP_005274033.1:p.Arg297Lys
|
|
XM_017017669.2:c.-122G>A
|
XP_016873158.1:n.-122G>A
|
|
XM_017017670.2:c.-122G>A
|
XP_016873159.1:n.-122G>A
|
|
XM_017017671.2:c.890G>A
|
XP_016873160.1:p.Arg297Lys
|
|
XR_949903.3:n.988G>A
|
|
|
NM_002180.3:c.890G>A
MANE Select
|
NP_002171.2:p.Arg297Lys
|
|