ENST00000262304.9:c.3631G>A
MANE Select
|
ENSP00000262304.4:p.Glu1211Lys
|
|
ENST00000262304.8:c.3631G>A
|
ENSP00000262304.4:p.Glu1211Lys
|
|
ENST00000415938.7:n.310+804G>A
|
|
|
ENST00000423118.5:c.3631G>A
|
ENSP00000399501.1:p.Glu1211Lys
|
|
ENST00000468674.5:n.430+804G>A
|
|
|
ENST00000469241.2:n.581G>A
|
|
|
ENST00000483024.1:c.233+280G>A
|
|
|
ENST00000483731.5:n.790+804G>A
|
|
|
ENST00000488185.2:c.473-3178G>A
|
|
|
ENST00000565639.6:n.773+804G>A
|
|
|
ENST00000568591.5:c.2226+804G>A
|
ENSP00000457162.1:n.2226+804G>A
|
|
ENST00000569983.5:n.421+804G>A
|
|
|
NM_000296.3:c.3631G>A
|
NP_000287.3:p.Glu1211Lys
|
|
NM_001009944.2:c.3631G>A
|
NP_001009944.2:p.Glu1211Lys
|
|
XM_005255370.2:c.586G>A
|
XP_005255427.1:p.Glu196Lys
|
|
XM_011522525.1:c.3709G>A
|
XP_011520827.1:p.Glu1237Lys
|
|
XM_011522526.1:c.3709G>A
|
XP_011520828.1:p.Glu1237Lys
|
|
XM_011522527.1:c.3709G>A
|
XP_011520829.1:p.Glu1237Lys
|
|
XM_011522528.1:c.3685G>A
|
XP_011520830.1:p.Glu1229Lys
|
|
XM_011522529.1:c.3685G>A
|
XP_011520831.1:p.Glu1229Lys
|
|
XM_011522530.1:c.3655G>A
|
XP_011520832.1:p.Glu1219Lys
|
|
XM_011522531.1:c.3637G>A
|
XP_011520833.1:p.Glu1213Lys
|
|
XM_011522532.1:c.3583G>A
|
XP_011520834.1:p.Glu1195Lys
|
|
XM_011522533.1:c.3502G>A
|
XP_011520835.1:p.Glu1168Lys
|
|
XM_011522534.1:c.3445G>A
|
XP_011520836.1:p.Glu1149Lys
|
|
XM_011522535.1:c.1531G>A
|
XP_011520837.1:p.Glu511Lys
|
|
XM_011522536.1:c.3709G>A
|
XP_011520838.1:p.Glu1237Lys
|
|
XM_011522537.1:c.709G>A
|
XP_011520839.1:p.Glu237Lys
|
|
XR_932867.1:n.3724G>A
|
|
|
XR_932868.1:n.3724G>A
|
|
|
XR_932869.1:n.3724G>A
|
|
|
XR_932870.1:n.3724G>A
|
|
|
XM_005255370.3:c.586G>A
|
XP_005255427.1:p.Glu196Lys
|
|
XM_011522528.3:c.3685G>A
|
XP_011520830.1:p.Glu1229Lys
|
|
XM_011522529.2:c.3685G>A
|
XP_011520831.1:p.Glu1229Lys
|
|
XM_011522537.2:c.709G>A
|
XP_011520839.1:p.Glu237Lys
|
|
XM_024450298.1:c.3751G>A
|
XP_024306066.1:p.Glu1251Lys
|
|
XM_024450299.1:c.3679G>A
|
XP_024306067.1:p.Glu1227Lys
|
|
XM_024450300.1:c.3541G>A
|
XP_024306068.1:p.Glu1181Lys
|
|
XM_024450301.1:c.1627G>A
|
XP_024306069.1:p.Glu543Lys
|
|
NM_000296.4:c.3631G>A
|
NP_000287.4:p.Glu1211Lys
|
|
NM_001009944.3:c.3631G>A
MANE Select
|
NP_001009944.3:p.Glu1211Lys
|
|