ENST00000264380.9:c.3450A>G
MANE Select
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ENSP00000264380.4:p.Arg1150=
|
|
ENST00000264380.8:c.3450A>G
|
ENSP00000264380.4:p.Arg1150=
|
|
ENST00000452564.1:c.3282A>G
|
ENSP00000405736.1:p.Arg1094=
|
|
NM_015040.3:c.3450A>G
|
NP_055855.2:p.Arg1150=
|
|
XM_011510778.1:c.3486A>G
|
XP_011509080.1:p.Arg1162=
|
|
XM_011510779.1:c.3486A>G
|
XP_011509081.1:p.Arg1162=
|
|
XM_011510780.1:c.3483A>G
|
XP_011509082.1:p.Arg1161=
|
|
XM_011510781.1:c.3468A>G
|
XP_011509083.1:p.Arg1156=
|
|
XM_011510782.1:c.3486A>G
|
XP_011509084.1:p.Arg1162=
|
|
XM_011510783.1:c.3318A>G
|
XP_011509085.1:p.Arg1106=
|
|
XM_011510784.1:c.3315A>G
|
XP_011509086.1:p.Arg1105=
|
|
XM_011510785.1:c.3300A>G
|
XP_011509087.1:p.Arg1100=
|
|
XM_011510786.1:c.3195A>G
|
XP_011509088.1:p.Arg1065=
|
|
XM_011510787.1:c.3192A>G
|
XP_011509089.1:p.Arg1064=
|
|
XM_011510788.1:c.3159A>G
|
XP_011509090.1:p.Arg1053=
|
|
XM_011510789.1:c.3009A>G
|
XP_011509091.1:p.Arg1003=
|
|
XM_011510790.1:c.2493A>G
|
XP_011509092.1:p.Arg831=
|
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XM_011510791.1:c.2493A>G
|
XP_011509093.1:p.Arg831=
|
|
XM_011510792.1:c.3486A>G
|
XP_011509094.1:p.Arg1162=
|
|
XR_922888.1:n.3623A>G
|
|
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XM_011510778.3:c.3486A>G
|
XP_011509080.1:p.Arg1162=
|
|
XM_011510779.2:c.3486A>G
|
XP_011509081.1:p.Arg1162=
|
|
XM_011510780.2:c.3483A>G
|
XP_011509082.1:p.Arg1161=
|
|
XM_011510781.3:c.3468A>G
|
XP_011509083.1:p.Arg1156=
|
|
XM_011510782.3:c.3486A>G
|
XP_011509084.1:p.Arg1162=
|
|
XM_011510783.3:c.3318A>G
|
XP_011509085.1:p.Arg1106=
|
|
XM_011510784.2:c.3315A>G
|
XP_011509086.1:p.Arg1105=
|
|
XM_011510785.3:c.3300A>G
|
XP_011509087.1:p.Arg1100=
|
|
XM_011510786.3:c.3195A>G
|
XP_011509088.1:p.Arg1065=
|
|
XM_011510789.2:c.3009A>G
|
XP_011509091.1:p.Arg1003=
|
|
XM_011510792.3:c.3486A>G
|
XP_011509094.1:p.Arg1162=
|
|
XM_017003568.1:c.3432A>G
|
XP_016859057.1:p.Arg1144=
|
|
XM_017003569.1:c.3264A>G
|
XP_016859058.1:p.Arg1088=
|
|
XM_017003570.1:c.2991A>G
|
XP_016859059.1:p.Arg997=
|
|
XM_017003571.1:c.2841A>G
|
XP_016859060.1:p.Arg947=
|
|
XM_017003572.1:c.2493A>G
|
XP_016859061.1:p.Arg831=
|
|
XM_017003573.1:c.2493A>G
|
XP_016859062.1:p.Arg831=
|
|
XM_017003574.1:c.2493A>G
|
XP_016859063.1:p.Arg831=
|
|
NM_015040.4:c.3450A>G
MANE Select
|
NP_055855.2:p.Arg1150=
|
|