ENST00000262304.9:c.3516G>C
MANE Select
|
ENSP00000262304.4:p.Gln1172His
|
|
ENST00000262304.8:c.3516G>C
|
ENSP00000262304.4:p.Gln1172His
|
|
ENST00000415938.7:n.310+689G>C
|
|
|
ENST00000423118.5:c.3516G>C
|
ENSP00000399501.1:p.Gln1172His
|
|
ENST00000468674.5:n.430+689G>C
|
|
|
ENST00000469241.2:n.466G>C
|
|
|
ENST00000483024.1:c.233+165G>C
|
|
|
ENST00000483731.5:n.790+689G>C
|
|
|
ENST00000488185.2:c.473-3293G>C
|
|
|
ENST00000565639.6:n.773+689G>C
|
|
|
ENST00000568591.5:c.2226+689G>C
|
ENSP00000457162.1:n.2226+689G>C
|
|
ENST00000569983.5:n.421+689G>C
|
|
|
NM_000296.3:c.3516G>C
|
NP_000287.3:p.Gln1172His
|
|
NM_001009944.2:c.3516G>C
|
NP_001009944.2:p.Gln1172His
|
|
XM_005255370.2:c.471G>C
|
XP_005255427.1:p.Gln157His
|
|
XM_011522525.1:c.3594G>C
|
XP_011520827.1:p.Gln1198His
|
|
XM_011522526.1:c.3594G>C
|
XP_011520828.1:p.Gln1198His
|
|
XM_011522527.1:c.3594G>C
|
XP_011520829.1:p.Gln1198His
|
|
XM_011522528.1:c.3570G>C
|
XP_011520830.1:p.Gln1190His
|
|
XM_011522529.1:c.3570G>C
|
XP_011520831.1:p.Gln1190His
|
|
XM_011522530.1:c.3540G>C
|
XP_011520832.1:p.Gln1180His
|
|
XM_011522531.1:c.3522G>C
|
XP_011520833.1:p.Gln1174His
|
|
XM_011522532.1:c.3468G>C
|
XP_011520834.1:p.Gln1156His
|
|
XM_011522533.1:c.3387G>C
|
XP_011520835.1:p.Gln1129His
|
|
XM_011522534.1:c.3330G>C
|
XP_011520836.1:p.Gln1110His
|
|
XM_011522535.1:c.1416G>C
|
XP_011520837.1:p.Gln472His
|
|
XM_011522536.1:c.3594G>C
|
XP_011520838.1:p.Gln1198His
|
|
XM_011522537.1:c.594G>C
|
XP_011520839.1:p.Gln198His
|
|
XR_932867.1:n.3609G>C
|
|
|
XR_932868.1:n.3609G>C
|
|
|
XR_932869.1:n.3609G>C
|
|
|
XR_932870.1:n.3609G>C
|
|
|
XM_005255370.3:c.471G>C
|
XP_005255427.1:p.Gln157His
|
|
XM_011522528.3:c.3570G>C
|
XP_011520830.1:p.Gln1190His
|
|
XM_011522529.2:c.3570G>C
|
XP_011520831.1:p.Gln1190His
|
|
XM_011522537.2:c.594G>C
|
XP_011520839.1:p.Gln198His
|
|
XM_024450298.1:c.3636G>C
|
XP_024306066.1:p.Gln1212His
|
|
XM_024450299.1:c.3564G>C
|
XP_024306067.1:p.Gln1188His
|
|
XM_024450300.1:c.3426G>C
|
XP_024306068.1:p.Gln1142His
|
|
XM_024450301.1:c.1512G>C
|
XP_024306069.1:p.Gln504His
|
|
NM_000296.4:c.3516G>C
|
NP_000287.4:p.Gln1172His
|
|
NM_001009944.3:c.3516G>C
MANE Select
|
NP_001009944.3:p.Gln1172His
|
|