ENST00000475668.6:c.2452G>C
MANE Select
|
ENSP00000417515.2:p.Gly818Arg
|
|
ENST00000549489.6:c.2452G>C
|
ENSP00000447378.2:p.Gly818Arg
|
|
ENST00000620571.1:c.2452G>C
|
ENSP00000482292.1:p.Gly818Arg
|
|
NM_004668.2:c.2452G>C
|
NP_004659.2:p.Gly818Arg
|
|
XM_006716168.2:c.2452G>C
|
XP_006716231.1:p.Gly818Arg
|
|
XM_011516670.1:c.2452G>C
|
XP_011514972.1:p.Gly818Arg
|
|
XM_011516671.1:c.2452G>C
|
XP_011514973.1:p.Gly818Arg
|
|
XM_011516672.1:c.2452G>C
|
XP_011514974.1:p.Gly818Arg
|
|
XM_011516673.1:c.2452G>C
|
XP_011514975.1:p.Gly818Arg
|
|
XM_011516674.1:c.2452G>C
|
XP_011514976.1:p.Gly818Arg
|
|
XR_927545.1:n.2564G>C
|
|
|
NM_001365693.1:c.2452G>C
MANE Select
|
NP_001352622.1:p.Gly818Arg
|
|
XM_011516670.2:c.2452G>C
|
XP_011514972.1:p.Gly818Arg
|
|
XM_011516671.2:c.2452G>C
|
XP_011514973.1:p.Gly818Arg
|
|
XM_011516672.2:c.2452G>C
|
XP_011514974.1:p.Gly818Arg
|
|
XM_011516673.2:c.2452G>C
|
XP_011514975.1:p.Gly818Arg
|
|
XM_011516674.2:c.2452G>C
|
XP_011514976.1:p.Gly818Arg
|
|
XM_017012772.1:c.2452G>C
|
XP_016868261.1:p.Gly818Arg
|
|
XM_024446990.1:c.2452G>C
|
XP_024302758.1:p.Gly818Arg
|
|
NM_004668.3:c.2452G>C
|
NP_004659.2:p.Gly818Arg
|
|