ENST00000262304.9:c.7269C>A
MANE Select
|
ENSP00000262304.4:p.Ser2423=
|
|
ENST00000262304.8:c.7269C>A
|
ENSP00000262304.4:p.Ser2423=
|
|
ENST00000415938.7:n.514C>A
|
|
|
ENST00000423118.5:c.7269C>A
|
ENSP00000399501.1:p.Ser2423=
|
|
ENST00000483024.1:c.437C>A
|
|
|
ENST00000483558.5:n.328C>A
|
|
|
ENST00000483731.5:n.994C>A
|
|
|
ENST00000486339.6:n.1015C>A
|
|
|
ENST00000487932.5:c.1956C>A
|
ENSP00000457132.1:p.Ser652=
|
|
ENST00000496574.6:n.1272C>A
|
|
|
ENST00000565639.6:n.977C>A
|
|
|
ENST00000568591.5:c.2430C>A
|
ENSP00000457162.1:n.2430C>A
|
|
ENST00000569983.5:n.625C>A
|
|
|
NM_000296.3:c.7269C>A
|
NP_000287.3:p.Ser2423=
|
|
NM_001009944.2:c.7269C>A
|
NP_001009944.2:p.Ser2423=
|
|
XM_005255370.2:c.4224C>A
|
XP_005255427.1:p.Ser1408=
|
|
XM_011522525.1:c.7347C>A
|
XP_011520827.1:p.Ser2449=
|
|
XM_011522526.1:c.7347C>A
|
XP_011520828.1:p.Ser2449=
|
|
XM_011522527.1:c.7347C>A
|
XP_011520829.1:p.Ser2449=
|
|
XM_011522528.1:c.7323C>A
|
XP_011520830.1:p.Ser2441=
|
|
XM_011522529.1:c.7323C>A
|
XP_011520831.1:p.Ser2441=
|
|
XM_011522530.1:c.7293C>A
|
XP_011520832.1:p.Ser2431=
|
|
XM_011522531.1:c.7275C>A
|
XP_011520833.1:p.Ser2425=
|
|
XM_011522532.1:c.7221C>A
|
XP_011520834.1:p.Ser2407=
|
|
XM_011522533.1:c.7140C>A
|
XP_011520835.1:p.Ser2380=
|
|
XM_011522534.1:c.7083C>A
|
XP_011520836.1:p.Ser2361=
|
|
XM_011522535.1:c.5169C>A
|
XP_011520837.1:p.Ser1723=
|
|
XM_011522536.1:c.7347C>A
|
XP_011520838.1:p.Ser2449=
|
|
XM_011522537.1:c.4347C>A
|
XP_011520839.1:p.Ser1449=
|
|
XR_932867.1:n.7362C>A
|
|
|
XR_932868.1:n.7362C>A
|
|
|
XR_932869.1:n.7362C>A
|
|
|
XR_932870.1:n.7362C>A
|
|
|
XM_005255370.3:c.4224C>A
|
XP_005255427.1:p.Ser1408=
|
|
XM_011522528.3:c.7323C>A
|
XP_011520830.1:p.Ser2441=
|
|
XM_011522529.2:c.7323C>A
|
XP_011520831.1:p.Ser2441=
|
|
XM_011522537.2:c.4347C>A
|
XP_011520839.1:p.Ser1449=
|
|
XM_024450298.1:c.7389C>A
|
XP_024306066.1:p.Ser2463=
|
|
XM_024450299.1:c.7317C>A
|
XP_024306067.1:p.Ser2439=
|
|
XM_024450300.1:c.7179C>A
|
XP_024306068.1:p.Ser2393=
|
|
XM_024450301.1:c.5265C>A
|
XP_024306069.1:p.Ser1755=
|
|
NM_000296.4:c.7269C>A
|
NP_000287.4:p.Ser2423=
|
|
NM_001009944.3:c.7269C>A
MANE Select
|
NP_001009944.3:p.Ser2423=
|
|