ENST00000262304.9:c.959C>T
MANE Select
|
ENSP00000262304.4:p.Ala320Val
|
|
ENST00000262304.8:c.959C>T
|
ENSP00000262304.4:p.Ala320Val
|
|
ENST00000423118.5:c.959C>T
|
ENSP00000399501.1:p.Ala320Val
|
|
ENST00000488185.2:c.46C>T
|
|
|
ENST00000570150.1:n.92C>T
|
|
|
NM_000296.3:c.959C>T
|
NP_000287.3:p.Ala320Val
|
|
NM_001009944.2:c.959C>T
|
NP_001009944.2:p.Ala320Val
|
|
XM_011522525.1:c.1013C>T
|
XP_011520827.1:p.Ala338Val
|
|
XM_011522526.1:c.1013C>T
|
XP_011520828.1:p.Ala338Val
|
|
XM_011522527.1:c.1013C>T
|
XP_011520829.1:p.Ala338Val
|
|
XM_011522528.1:c.1013C>T
|
XP_011520830.1:p.Ala338Val
|
|
XM_011522529.1:c.1013C>T
|
XP_011520831.1:p.Ala338Val
|
|
XM_011522530.1:c.959C>T
|
XP_011520832.1:p.Ala320Val
|
|
XM_011522531.1:c.941C>T
|
XP_011520833.1:p.Ala314Val
|
|
XM_011522532.1:c.887C>T
|
XP_011520834.1:p.Ala296Val
|
|
XM_011522533.1:c.806C>T
|
XP_011520835.1:p.Ala269Val
|
|
XM_011522534.1:c.749C>T
|
XP_011520836.1:p.Ala250Val
|
|
XM_011522536.1:c.1013C>T
|
XP_011520838.1:p.Ala338Val
|
|
XR_932867.1:n.1028C>T
|
|
|
XR_932868.1:n.1028C>T
|
|
|
XR_932869.1:n.1028C>T
|
|
|
XR_932870.1:n.1028C>T
|
|
|
XM_011522528.3:c.1013C>T
|
XP_011520830.1:p.Ala338Val
|
|
XM_011522529.2:c.1013C>T
|
XP_011520831.1:p.Ala338Val
|
|
XM_024450298.1:c.959C>T
|
XP_024306066.1:p.Ala320Val
|
|
XM_024450299.1:c.887C>T
|
XP_024306067.1:p.Ala296Val
|
|
XM_024450300.1:c.749C>T
|
XP_024306068.1:p.Ala250Val
|
|
NM_000296.4:c.959C>T
|
NP_000287.4:p.Ala320Val
|
|
NM_001009944.3:c.959C>T
MANE Select
|
NP_001009944.3:p.Ala320Val
|
|