ENST00000262304.9:c.7226C>T
MANE Select
|
ENSP00000262304.4:p.Thr2409Met
|
|
ENST00000262304.8:c.7226C>T
|
ENSP00000262304.4:p.Thr2409Met
|
|
ENST00000415938.7:n.471C>T
|
|
|
ENST00000423118.5:c.7226C>T
|
ENSP00000399501.1:p.Thr2409Met
|
|
ENST00000483024.1:c.394C>T
|
|
|
ENST00000483558.5:n.285C>T
|
|
|
ENST00000483731.5:n.951C>T
|
|
|
ENST00000486339.6:n.972C>T
|
|
|
ENST00000487932.5:c.1913C>T
|
ENSP00000457132.1:p.Thr638Met
|
|
ENST00000496574.6:n.1229C>T
|
|
|
ENST00000565639.6:n.934C>T
|
|
|
ENST00000568591.5:c.2387C>T
|
ENSP00000457162.1:n.2387C>T
|
|
ENST00000569983.5:n.582C>T
|
|
|
NM_000296.3:c.7226C>T
|
NP_000287.3:p.Thr2409Met
|
|
NM_001009944.2:c.7226C>T
|
NP_001009944.2:p.Thr2409Met
|
|
XM_005255370.2:c.4181C>T
|
XP_005255427.1:p.Thr1394Met
|
|
XM_011522525.1:c.7304C>T
|
XP_011520827.1:p.Thr2435Met
|
|
XM_011522526.1:c.7304C>T
|
XP_011520828.1:p.Thr2435Met
|
|
XM_011522527.1:c.7304C>T
|
XP_011520829.1:p.Thr2435Met
|
|
XM_011522528.1:c.7280C>T
|
XP_011520830.1:p.Thr2427Met
|
|
XM_011522529.1:c.7280C>T
|
XP_011520831.1:p.Thr2427Met
|
|
XM_011522530.1:c.7250C>T
|
XP_011520832.1:p.Thr2417Met
|
|
XM_011522531.1:c.7232C>T
|
XP_011520833.1:p.Thr2411Met
|
|
XM_011522532.1:c.7178C>T
|
XP_011520834.1:p.Thr2393Met
|
|
XM_011522533.1:c.7097C>T
|
XP_011520835.1:p.Thr2366Met
|
|
XM_011522534.1:c.7040C>T
|
XP_011520836.1:p.Thr2347Met
|
|
XM_011522535.1:c.5126C>T
|
XP_011520837.1:p.Thr1709Met
|
|
XM_011522536.1:c.7304C>T
|
XP_011520838.1:p.Thr2435Met
|
|
XM_011522537.1:c.4304C>T
|
XP_011520839.1:p.Thr1435Met
|
|
XR_932867.1:n.7319C>T
|
|
|
XR_932868.1:n.7319C>T
|
|
|
XR_932869.1:n.7319C>T
|
|
|
XR_932870.1:n.7319C>T
|
|
|
XM_005255370.3:c.4181C>T
|
XP_005255427.1:p.Thr1394Met
|
|
XM_011522528.3:c.7280C>T
|
XP_011520830.1:p.Thr2427Met
|
|
XM_011522529.2:c.7280C>T
|
XP_011520831.1:p.Thr2427Met
|
|
XM_011522537.2:c.4304C>T
|
XP_011520839.1:p.Thr1435Met
|
|
XM_024450298.1:c.7346C>T
|
XP_024306066.1:p.Thr2449Met
|
|
XM_024450299.1:c.7274C>T
|
XP_024306067.1:p.Thr2425Met
|
|
XM_024450300.1:c.7136C>T
|
XP_024306068.1:p.Thr2379Met
|
|
XM_024450301.1:c.5222C>T
|
XP_024306069.1:p.Thr1741Met
|
|
NM_000296.4:c.7226C>T
|
NP_000287.4:p.Thr2409Met
|
|
NM_001009944.3:c.7226C>T
MANE Select
|
NP_001009944.3:p.Thr2409Met
|
|