ENST00000264380.9:c.3455T>G
MANE Select
|
ENSP00000264380.4:p.Leu1152Arg
|
|
ENST00000264380.8:c.3455T>G
|
ENSP00000264380.4:p.Leu1152Arg
|
|
ENST00000452564.1:c.3287T>G
|
ENSP00000405736.1:p.Leu1096Arg
|
|
NM_015040.3:c.3455T>G
|
NP_055855.2:p.Leu1152Arg
|
|
XM_011510778.1:c.3491T>G
|
XP_011509080.1:p.Leu1164Arg
|
|
XM_011510779.1:c.3491T>G
|
XP_011509081.1:p.Leu1164Arg
|
|
XM_011510780.1:c.3488T>G
|
XP_011509082.1:p.Leu1163Arg
|
|
XM_011510781.1:c.3473T>G
|
XP_011509083.1:p.Leu1158Arg
|
|
XM_011510782.1:c.3491T>G
|
XP_011509084.1:p.Leu1164Arg
|
|
XM_011510783.1:c.3323T>G
|
XP_011509085.1:p.Leu1108Arg
|
|
XM_011510784.1:c.3320T>G
|
XP_011509086.1:p.Leu1107Arg
|
|
XM_011510785.1:c.3305T>G
|
XP_011509087.1:p.Leu1102Arg
|
|
XM_011510786.1:c.3200T>G
|
XP_011509088.1:p.Leu1067Arg
|
|
XM_011510787.1:c.3197T>G
|
XP_011509089.1:p.Leu1066Arg
|
|
XM_011510788.1:c.3164T>G
|
XP_011509090.1:p.Leu1055Arg
|
|
XM_011510789.1:c.3014T>G
|
XP_011509091.1:p.Leu1005Arg
|
|
XM_011510790.1:c.2498T>G
|
XP_011509092.1:p.Leu833Arg
|
|
XM_011510791.1:c.2498T>G
|
XP_011509093.1:p.Leu833Arg
|
|
XM_011510792.1:c.3491T>G
|
XP_011509094.1:p.Leu1164Arg
|
|
XR_922888.1:n.3628T>G
|
|
|
XM_011510778.3:c.3491T>G
|
XP_011509080.1:p.Leu1164Arg
|
|
XM_011510779.2:c.3491T>G
|
XP_011509081.1:p.Leu1164Arg
|
|
XM_011510780.2:c.3488T>G
|
XP_011509082.1:p.Leu1163Arg
|
|
XM_011510781.3:c.3473T>G
|
XP_011509083.1:p.Leu1158Arg
|
|
XM_011510782.3:c.3491T>G
|
XP_011509084.1:p.Leu1164Arg
|
|
XM_011510783.3:c.3323T>G
|
XP_011509085.1:p.Leu1108Arg
|
|
XM_011510784.2:c.3320T>G
|
XP_011509086.1:p.Leu1107Arg
|
|
XM_011510785.3:c.3305T>G
|
XP_011509087.1:p.Leu1102Arg
|
|
XM_011510786.3:c.3200T>G
|
XP_011509088.1:p.Leu1067Arg
|
|
XM_011510789.2:c.3014T>G
|
XP_011509091.1:p.Leu1005Arg
|
|
XM_011510792.3:c.3491T>G
|
XP_011509094.1:p.Leu1164Arg
|
|
XM_017003568.1:c.3437T>G
|
XP_016859057.1:p.Leu1146Arg
|
|
XM_017003569.1:c.3269T>G
|
XP_016859058.1:p.Leu1090Arg
|
|
XM_017003570.1:c.2996T>G
|
XP_016859059.1:p.Leu999Arg
|
|
XM_017003571.1:c.2846T>G
|
XP_016859060.1:p.Leu949Arg
|
|
XM_017003572.1:c.2498T>G
|
XP_016859061.1:p.Leu833Arg
|
|
XM_017003573.1:c.2498T>G
|
XP_016859062.1:p.Leu833Arg
|
|
XM_017003574.1:c.2498T>G
|
XP_016859063.1:p.Leu833Arg
|
|
NM_015040.4:c.3455T>G
MANE Select
|
NP_055855.2:p.Leu1152Arg
|
|