ENST00000262304.9:c.3627T>A
MANE Select
|
ENSP00000262304.4:p.Phe1209Leu
|
|
ENST00000262304.8:c.3627T>A
|
ENSP00000262304.4:p.Phe1209Leu
|
|
ENST00000415938.7:n.310+800T>A
|
|
|
ENST00000423118.5:c.3627T>A
|
ENSP00000399501.1:p.Phe1209Leu
|
|
ENST00000468674.5:n.430+800T>A
|
|
|
ENST00000469241.2:n.577T>A
|
|
|
ENST00000483024.1:c.233+276T>A
|
|
|
ENST00000483731.5:n.790+800T>A
|
|
|
ENST00000488185.2:c.473-3182T>A
|
|
|
ENST00000565639.6:n.773+800T>A
|
|
|
ENST00000568591.5:c.2226+800T>A
|
ENSP00000457162.1:n.2226+800T>A
|
|
ENST00000569983.5:n.421+800T>A
|
|
|
NM_000296.3:c.3627T>A
|
NP_000287.3:p.Phe1209Leu
|
|
NM_001009944.2:c.3627T>A
|
NP_001009944.2:p.Phe1209Leu
|
|
XM_005255370.2:c.582T>A
|
XP_005255427.1:p.Phe194Leu
|
|
XM_011522525.1:c.3705T>A
|
XP_011520827.1:p.Phe1235Leu
|
|
XM_011522526.1:c.3705T>A
|
XP_011520828.1:p.Phe1235Leu
|
|
XM_011522527.1:c.3705T>A
|
XP_011520829.1:p.Phe1235Leu
|
|
XM_011522528.1:c.3681T>A
|
XP_011520830.1:p.Phe1227Leu
|
|
XM_011522529.1:c.3681T>A
|
XP_011520831.1:p.Phe1227Leu
|
|
XM_011522530.1:c.3651T>A
|
XP_011520832.1:p.Phe1217Leu
|
|
XM_011522531.1:c.3633T>A
|
XP_011520833.1:p.Phe1211Leu
|
|
XM_011522532.1:c.3579T>A
|
XP_011520834.1:p.Phe1193Leu
|
|
XM_011522533.1:c.3498T>A
|
XP_011520835.1:p.Phe1166Leu
|
|
XM_011522534.1:c.3441T>A
|
XP_011520836.1:p.Phe1147Leu
|
|
XM_011522535.1:c.1527T>A
|
XP_011520837.1:p.Phe509Leu
|
|
XM_011522536.1:c.3705T>A
|
XP_011520838.1:p.Phe1235Leu
|
|
XM_011522537.1:c.705T>A
|
XP_011520839.1:p.Phe235Leu
|
|
XR_932867.1:n.3720T>A
|
|
|
XR_932868.1:n.3720T>A
|
|
|
XR_932869.1:n.3720T>A
|
|
|
XR_932870.1:n.3720T>A
|
|
|
XM_005255370.3:c.582T>A
|
XP_005255427.1:p.Phe194Leu
|
|
XM_011522528.3:c.3681T>A
|
XP_011520830.1:p.Phe1227Leu
|
|
XM_011522529.2:c.3681T>A
|
XP_011520831.1:p.Phe1227Leu
|
|
XM_011522537.2:c.705T>A
|
XP_011520839.1:p.Phe235Leu
|
|
XM_024450298.1:c.3747T>A
|
XP_024306066.1:p.Phe1249Leu
|
|
XM_024450299.1:c.3675T>A
|
XP_024306067.1:p.Phe1225Leu
|
|
XM_024450300.1:c.3537T>A
|
XP_024306068.1:p.Phe1179Leu
|
|
XM_024450301.1:c.1623T>A
|
XP_024306069.1:p.Phe541Leu
|
|
NM_000296.4:c.3627T>A
|
NP_000287.4:p.Phe1209Leu
|
|
NM_001009944.3:c.3627T>A
MANE Select
|
NP_001009944.3:p.Phe1209Leu
|
|