ENST00000262304.9:c.5538C>T
MANE Select
|
ENSP00000262304.4:p.Ser1846=
|
|
ENST00000262304.8:c.5538C>T
|
ENSP00000262304.4:p.Ser1846=
|
|
ENST00000415938.7:n.311-2681C>T
|
|
|
ENST00000423118.5:c.5538C>T
|
ENSP00000399501.1:p.Ser1846=
|
|
ENST00000468674.5:n.431-279C>T
|
|
|
ENST00000483024.1:c.233+2187C>T
|
|
|
ENST00000483731.5:n.791-2681C>T
|
|
|
ENST00000487932.5:c.225C>T
|
ENSP00000457132.1:p.Ser75=
|
|
ENST00000488185.2:c.473-1271C>T
|
|
|
ENST00000565639.6:n.774-2681C>T
|
|
|
ENST00000568591.5:c.2227-2681C>T
|
ENSP00000457162.1:n.2227-2681C>T
|
|
ENST00000569983.5:n.422-2681C>T
|
|
|
NM_000296.3:c.5538C>T
|
NP_000287.3:p.Ser1846=
|
|
NM_001009944.2:c.5538C>T
|
NP_001009944.2:p.Ser1846=
|
|
XM_005255370.2:c.2493C>T
|
XP_005255427.1:p.Ser831=
|
|
XM_011522525.1:c.5616C>T
|
XP_011520827.1:p.Ser1872=
|
|
XM_011522526.1:c.5616C>T
|
XP_011520828.1:p.Ser1872=
|
|
XM_011522527.1:c.5616C>T
|
XP_011520829.1:p.Ser1872=
|
|
XM_011522528.1:c.5592C>T
|
XP_011520830.1:p.Ser1864=
|
|
XM_011522529.1:c.5592C>T
|
XP_011520831.1:p.Ser1864=
|
|
XM_011522530.1:c.5562C>T
|
XP_011520832.1:p.Ser1854=
|
|
XM_011522531.1:c.5544C>T
|
XP_011520833.1:p.Ser1848=
|
|
XM_011522532.1:c.5490C>T
|
XP_011520834.1:p.Ser1830=
|
|
XM_011522533.1:c.5409C>T
|
XP_011520835.1:p.Ser1803=
|
|
XM_011522534.1:c.5352C>T
|
XP_011520836.1:p.Ser1784=
|
|
XM_011522535.1:c.3438C>T
|
XP_011520837.1:p.Ser1146=
|
|
XM_011522536.1:c.5616C>T
|
XP_011520838.1:p.Ser1872=
|
|
XM_011522537.1:c.2616C>T
|
XP_011520839.1:p.Ser872=
|
|
XR_932867.1:n.5631C>T
|
|
|
XR_932868.1:n.5631C>T
|
|
|
XR_932869.1:n.5631C>T
|
|
|
XR_932870.1:n.5631C>T
|
|
|
XM_005255370.3:c.2493C>T
|
XP_005255427.1:p.Ser831=
|
|
XM_011522528.3:c.5592C>T
|
XP_011520830.1:p.Ser1864=
|
|
XM_011522529.2:c.5592C>T
|
XP_011520831.1:p.Ser1864=
|
|
XM_011522537.2:c.2616C>T
|
XP_011520839.1:p.Ser872=
|
|
XM_024450298.1:c.5658C>T
|
XP_024306066.1:p.Ser1886=
|
|
XM_024450299.1:c.5586C>T
|
XP_024306067.1:p.Ser1862=
|
|
XM_024450300.1:c.5448C>T
|
XP_024306068.1:p.Ser1816=
|
|
XM_024450301.1:c.3534C>T
|
XP_024306069.1:p.Ser1178=
|
|
NM_000296.4:c.5538C>T
|
NP_000287.4:p.Ser1846=
|
|
NM_001009944.3:c.5538C>T
MANE Select
|
NP_001009944.3:p.Ser1846=
|
|