ENST00000681617.1:c.838G=
|
ENSP00000505544.1:p.Asp280=
|
|
ENST00000681780.1:c.295G=
|
ENSP00000505780.1:p.Asp99=
|
|
ENST00000370131.3:c.838G=
|
ENSP00000359150.3:p.Asp280=
|
|
ENST00000370132.8:c.838G=
MANE Select
|
ENSP00000359151.3:p.Asp280=
|
|
NM_001918.3:c.838G=
|
NP_001909.3:p.Asp280=
|
|
XM_005270545.2:c.295G=
|
XP_005270602.1:p.Asp99=
|
|
XM_005270546.2:c.295G=
|
XP_005270603.1:p.Asp99=
|
|
XR_946560.1:n.858G=
|
|
|
XM_005270545.4:c.295G=
|
XP_005270602.1:p.Asp99=
|
|
XM_017000468.2:c.295G=
|
XP_016855957.1:p.Asp99=
|
|
XM_017000469.2:c.295G=
|
XP_016855958.1:p.Asp99=
|
|
XR_946560.3:n.855G=
|
|
|
NM_001918.4:c.838G=
|
NP_001909.3:p.Asp280=
|
|
NM_001918.5:c.838G=
MANE Select
|
NP_001909.4:p.Asp280=
|
|
NM_001399969.1:c.295G=
|
NP_001386898.1:p.Asp99=
|
|
NM_001399972.1:c.295G=
|
NP_001386901.1:p.Asp99=
|
|
NR_174363.1:n.670G=
|
|
|
NR_174364.1:n.852G=
|
|
|
NR_174365.1:n.635G=
|
|
|
NR_174366.1:n.852G=
|
|
|