ENST00000262304.9:c.8196G>A
MANE Select
|
ENSP00000262304.4:p.Arg2732=
|
|
ENST00000262304.8:c.8196G>A
|
ENSP00000262304.4:p.Arg2732=
|
|
ENST00000415938.7:n.1441G>A
|
|
|
ENST00000423118.5:c.8196G>A
|
ENSP00000399501.1:p.Arg2732=
|
|
ENST00000483731.5:n.1921G>A
|
|
|
ENST00000486339.6:n.2332G>A
|
|
|
ENST00000487932.5:c.2883G>A
|
ENSP00000457132.1:p.Arg961=
|
|
ENST00000496574.6:n.2432G>A
|
|
|
ENST00000561991.5:n.718G>A
|
|
|
ENST00000565639.6:n.1904G>A
|
|
|
ENST00000567946.1:c.257G>A
|
|
|
NM_000296.3:c.8196G>A
|
NP_000287.3:p.Arg2732=
|
|
NM_001009944.2:c.8196G>A
|
NP_001009944.2:p.Arg2732=
|
|
XM_005255370.2:c.5151G>A
|
XP_005255427.1:p.Arg1717=
|
|
XM_011522525.1:c.8274G>A
|
XP_011520827.1:p.Arg2758=
|
|
XM_011522526.1:c.8274G>A
|
XP_011520828.1:p.Arg2758=
|
|
XM_011522527.1:c.8274G>A
|
XP_011520829.1:p.Arg2758=
|
|
XM_011522528.1:c.8250G>A
|
XP_011520830.1:p.Arg2750=
|
|
XM_011522529.1:c.8250G>A
|
XP_011520831.1:p.Arg2750=
|
|
XM_011522530.1:c.8220G>A
|
XP_011520832.1:p.Arg2740=
|
|
XM_011522531.1:c.8202G>A
|
XP_011520833.1:p.Arg2734=
|
|
XM_011522532.1:c.8148G>A
|
XP_011520834.1:p.Arg2716=
|
|
XM_011522533.1:c.8067G>A
|
XP_011520835.1:p.Arg2689=
|
|
XM_011522534.1:c.8010G>A
|
XP_011520836.1:p.Arg2670=
|
|
XM_011522535.1:c.6096G>A
|
XP_011520837.1:p.Arg2032=
|
|
XM_011522536.1:c.8274G>A
|
XP_011520838.1:p.Arg2758=
|
|
XM_011522537.1:c.5274G>A
|
XP_011520839.1:p.Arg1758=
|
|
XR_932867.1:n.8289G>A
|
|
|
XR_932868.1:n.8289G>A
|
|
|
XR_932869.1:n.8289G>A
|
|
|
XR_932870.1:n.8289G>A
|
|
|
XM_005255370.3:c.5151G>A
|
XP_005255427.1:p.Arg1717=
|
|
XM_011522528.3:c.8250G>A
|
XP_011520830.1:p.Arg2750=
|
|
XM_011522529.2:c.8250G>A
|
XP_011520831.1:p.Arg2750=
|
|
XM_011522537.2:c.5274G>A
|
XP_011520839.1:p.Arg1758=
|
|
XM_024450298.1:c.8316G>A
|
XP_024306066.1:p.Arg2772=
|
|
XM_024450299.1:c.8244G>A
|
XP_024306067.1:p.Arg2748=
|
|
XM_024450300.1:c.8106G>A
|
XP_024306068.1:p.Arg2702=
|
|
XM_024450301.1:c.6192G>A
|
XP_024306069.1:p.Arg2064=
|
|
NM_000296.4:c.8196G>A
|
NP_000287.4:p.Arg2732=
|
|
NM_001009944.3:c.8196G>A
MANE Select
|
NP_001009944.3:p.Arg2732=
|
|