ENST00000262304.9:c.7336T>G
MANE Select
|
ENSP00000262304.4:p.Phe2446Val
|
|
ENST00000262304.8:c.7336T>G
|
ENSP00000262304.4:p.Phe2446Val
|
|
ENST00000415938.7:n.581T>G
|
|
|
ENST00000423118.5:c.7336T>G
|
ENSP00000399501.1:p.Phe2446Val
|
|
ENST00000483558.5:n.395T>G
|
|
|
ENST00000483731.5:n.1061T>G
|
|
|
ENST00000486339.6:n.1082T>G
|
|
|
ENST00000487932.5:c.2023T>G
|
ENSP00000457132.1:p.Phe675Val
|
|
ENST00000496574.6:n.1339T>G
|
|
|
ENST00000565639.6:n.1044T>G
|
|
|
ENST00000568591.5:c.2497T>G
|
ENSP00000457162.1:n.2497T>G
|
|
ENST00000569983.5:n.692T>G
|
|
|
NM_000296.3:c.7336T>G
|
NP_000287.3:p.Phe2446Val
|
|
NM_001009944.2:c.7336T>G
|
NP_001009944.2:p.Phe2446Val
|
|
XM_005255370.2:c.4291T>G
|
XP_005255427.1:p.Phe1431Val
|
|
XM_011522525.1:c.7414T>G
|
XP_011520827.1:p.Phe2472Val
|
|
XM_011522526.1:c.7414T>G
|
XP_011520828.1:p.Phe2472Val
|
|
XM_011522527.1:c.7414T>G
|
XP_011520829.1:p.Phe2472Val
|
|
XM_011522528.1:c.7390T>G
|
XP_011520830.1:p.Phe2464Val
|
|
XM_011522529.1:c.7390T>G
|
XP_011520831.1:p.Phe2464Val
|
|
XM_011522530.1:c.7360T>G
|
XP_011520832.1:p.Phe2454Val
|
|
XM_011522531.1:c.7342T>G
|
XP_011520833.1:p.Phe2448Val
|
|
XM_011522532.1:c.7288T>G
|
XP_011520834.1:p.Phe2430Val
|
|
XM_011522533.1:c.7207T>G
|
XP_011520835.1:p.Phe2403Val
|
|
XM_011522534.1:c.7150T>G
|
XP_011520836.1:p.Phe2384Val
|
|
XM_011522535.1:c.5236T>G
|
XP_011520837.1:p.Phe1746Val
|
|
XM_011522536.1:c.7414T>G
|
XP_011520838.1:p.Phe2472Val
|
|
XM_011522537.1:c.4414T>G
|
XP_011520839.1:p.Phe1472Val
|
|
XR_932867.1:n.7429T>G
|
|
|
XR_932868.1:n.7429T>G
|
|
|
XR_932869.1:n.7429T>G
|
|
|
XR_932870.1:n.7429T>G
|
|
|
XM_005255370.3:c.4291T>G
|
XP_005255427.1:p.Phe1431Val
|
|
XM_011522528.3:c.7390T>G
|
XP_011520830.1:p.Phe2464Val
|
|
XM_011522529.2:c.7390T>G
|
XP_011520831.1:p.Phe2464Val
|
|
XM_011522537.2:c.4414T>G
|
XP_011520839.1:p.Phe1472Val
|
|
XM_024450298.1:c.7456T>G
|
XP_024306066.1:p.Phe2486Val
|
|
XM_024450299.1:c.7384T>G
|
XP_024306067.1:p.Phe2462Val
|
|
XM_024450300.1:c.7246T>G
|
XP_024306068.1:p.Phe2416Val
|
|
XM_024450301.1:c.5332T>G
|
XP_024306069.1:p.Phe1778Val
|
|
NM_000296.4:c.7336T>G
|
NP_000287.4:p.Phe2446Val
|
|
NM_001009944.3:c.7336T>G
MANE Select
|
NP_001009944.3:p.Phe2446Val
|
|