ENST00000262304.9:c.7232G>C
MANE Select
|
ENSP00000262304.4:p.Ser2411Thr
|
|
ENST00000262304.8:c.7232G>C
|
ENSP00000262304.4:p.Ser2411Thr
|
|
ENST00000415938.7:n.477G>C
|
|
|
ENST00000423118.5:c.7232G>C
|
ENSP00000399501.1:p.Ser2411Thr
|
|
ENST00000483024.1:c.400G>C
|
|
|
ENST00000483558.5:n.291G>C
|
|
|
ENST00000483731.5:n.957G>C
|
|
|
ENST00000486339.6:n.978G>C
|
|
|
ENST00000487932.5:c.1919G>C
|
ENSP00000457132.1:p.Ser640Thr
|
|
ENST00000496574.6:n.1235G>C
|
|
|
ENST00000565639.6:n.940G>C
|
|
|
ENST00000568591.5:c.2393G>C
|
ENSP00000457162.1:n.2393G>C
|
|
ENST00000569983.5:n.588G>C
|
|
|
NM_000296.3:c.7232G>C
|
NP_000287.3:p.Ser2411Thr
|
|
NM_001009944.2:c.7232G>C
|
NP_001009944.2:p.Ser2411Thr
|
|
XM_005255370.2:c.4187G>C
|
XP_005255427.1:p.Ser1396Thr
|
|
XM_011522525.1:c.7310G>C
|
XP_011520827.1:p.Ser2437Thr
|
|
XM_011522526.1:c.7310G>C
|
XP_011520828.1:p.Ser2437Thr
|
|
XM_011522527.1:c.7310G>C
|
XP_011520829.1:p.Ser2437Thr
|
|
XM_011522528.1:c.7286G>C
|
XP_011520830.1:p.Ser2429Thr
|
|
XM_011522529.1:c.7286G>C
|
XP_011520831.1:p.Ser2429Thr
|
|
XM_011522530.1:c.7256G>C
|
XP_011520832.1:p.Ser2419Thr
|
|
XM_011522531.1:c.7238G>C
|
XP_011520833.1:p.Ser2413Thr
|
|
XM_011522532.1:c.7184G>C
|
XP_011520834.1:p.Ser2395Thr
|
|
XM_011522533.1:c.7103G>C
|
XP_011520835.1:p.Ser2368Thr
|
|
XM_011522534.1:c.7046G>C
|
XP_011520836.1:p.Ser2349Thr
|
|
XM_011522535.1:c.5132G>C
|
XP_011520837.1:p.Ser1711Thr
|
|
XM_011522536.1:c.7310G>C
|
XP_011520838.1:p.Ser2437Thr
|
|
XM_011522537.1:c.4310G>C
|
XP_011520839.1:p.Ser1437Thr
|
|
XR_932867.1:n.7325G>C
|
|
|
XR_932868.1:n.7325G>C
|
|
|
XR_932869.1:n.7325G>C
|
|
|
XR_932870.1:n.7325G>C
|
|
|
XM_005255370.3:c.4187G>C
|
XP_005255427.1:p.Ser1396Thr
|
|
XM_011522528.3:c.7286G>C
|
XP_011520830.1:p.Ser2429Thr
|
|
XM_011522529.2:c.7286G>C
|
XP_011520831.1:p.Ser2429Thr
|
|
XM_011522537.2:c.4310G>C
|
XP_011520839.1:p.Ser1437Thr
|
|
XM_024450298.1:c.7352G>C
|
XP_024306066.1:p.Ser2451Thr
|
|
XM_024450299.1:c.7280G>C
|
XP_024306067.1:p.Ser2427Thr
|
|
XM_024450300.1:c.7142G>C
|
XP_024306068.1:p.Ser2381Thr
|
|
XM_024450301.1:c.5228G>C
|
XP_024306069.1:p.Ser1743Thr
|
|
NM_000296.4:c.7232G>C
|
NP_000287.4:p.Ser2411Thr
|
|
NM_001009944.3:c.7232G>C
MANE Select
|
NP_001009944.3:p.Ser2411Thr
|
|