ENST00000264380.9:c.3414T>A
MANE Select
|
ENSP00000264380.4:p.Ile1138=
|
|
ENST00000264380.8:c.3414T>A
|
ENSP00000264380.4:p.Ile1138=
|
|
ENST00000452564.1:c.3246T>A
|
ENSP00000405736.1:p.Ile1082=
|
|
NM_015040.3:c.3414T>A
|
NP_055855.2:p.Ile1138=
|
|
XM_011510778.1:c.3450T>A
|
XP_011509080.1:p.Ile1150=
|
|
XM_011510779.1:c.3450T>A
|
XP_011509081.1:p.Ile1150=
|
|
XM_011510780.1:c.3447T>A
|
XP_011509082.1:p.Ile1149=
|
|
XM_011510781.1:c.3432T>A
|
XP_011509083.1:p.Ile1144=
|
|
XM_011510782.1:c.3450T>A
|
XP_011509084.1:p.Ile1150=
|
|
XM_011510783.1:c.3282T>A
|
XP_011509085.1:p.Ile1094=
|
|
XM_011510784.1:c.3279T>A
|
XP_011509086.1:p.Ile1093=
|
|
XM_011510785.1:c.3264T>A
|
XP_011509087.1:p.Ile1088=
|
|
XM_011510786.1:c.3159T>A
|
XP_011509088.1:p.Ile1053=
|
|
XM_011510787.1:c.3156T>A
|
XP_011509089.1:p.Ile1052=
|
|
XM_011510788.1:c.3123T>A
|
XP_011509090.1:p.Ile1041=
|
|
XM_011510789.1:c.2973T>A
|
XP_011509091.1:p.Ile991=
|
|
XM_011510790.1:c.2457T>A
|
XP_011509092.1:p.Ile819=
|
|
XM_011510791.1:c.2457T>A
|
XP_011509093.1:p.Ile819=
|
|
XM_011510792.1:c.3450T>A
|
XP_011509094.1:p.Ile1150=
|
|
XR_922888.1:n.3587T>A
|
|
|
XM_011510778.3:c.3450T>A
|
XP_011509080.1:p.Ile1150=
|
|
XM_011510779.2:c.3450T>A
|
XP_011509081.1:p.Ile1150=
|
|
XM_011510780.2:c.3447T>A
|
XP_011509082.1:p.Ile1149=
|
|
XM_011510781.3:c.3432T>A
|
XP_011509083.1:p.Ile1144=
|
|
XM_011510782.3:c.3450T>A
|
XP_011509084.1:p.Ile1150=
|
|
XM_011510783.3:c.3282T>A
|
XP_011509085.1:p.Ile1094=
|
|
XM_011510784.2:c.3279T>A
|
XP_011509086.1:p.Ile1093=
|
|
XM_011510785.3:c.3264T>A
|
XP_011509087.1:p.Ile1088=
|
|
XM_011510786.3:c.3159T>A
|
XP_011509088.1:p.Ile1053=
|
|
XM_011510789.2:c.2973T>A
|
XP_011509091.1:p.Ile991=
|
|
XM_011510792.3:c.3450T>A
|
XP_011509094.1:p.Ile1150=
|
|
XM_017003568.1:c.3396T>A
|
XP_016859057.1:p.Ile1132=
|
|
XM_017003569.1:c.3228T>A
|
XP_016859058.1:p.Ile1076=
|
|
XM_017003570.1:c.2955T>A
|
XP_016859059.1:p.Ile985=
|
|
XM_017003571.1:c.2805T>A
|
XP_016859060.1:p.Ile935=
|
|
XM_017003572.1:c.2457T>A
|
XP_016859061.1:p.Ile819=
|
|
XM_017003573.1:c.2457T>A
|
XP_016859062.1:p.Ile819=
|
|
XM_017003574.1:c.2457T>A
|
XP_016859063.1:p.Ile819=
|
|
NM_015040.4:c.3414T>A
MANE Select
|
NP_055855.2:p.Ile1138=
|
|