ENST00000264380.9:c.3449G>A
MANE Select
|
ENSP00000264380.4:p.Arg1150Lys
|
|
ENST00000264380.8:c.3449G>A
|
ENSP00000264380.4:p.Arg1150Lys
|
|
ENST00000452564.1:c.3281G>A
|
ENSP00000405736.1:p.Arg1094Lys
|
|
NM_015040.3:c.3449G>A
|
NP_055855.2:p.Arg1150Lys
|
|
XM_011510778.1:c.3485G>A
|
XP_011509080.1:p.Arg1162Lys
|
|
XM_011510779.1:c.3485G>A
|
XP_011509081.1:p.Arg1162Lys
|
|
XM_011510780.1:c.3482G>A
|
XP_011509082.1:p.Arg1161Lys
|
|
XM_011510781.1:c.3467G>A
|
XP_011509083.1:p.Arg1156Lys
|
|
XM_011510782.1:c.3485G>A
|
XP_011509084.1:p.Arg1162Lys
|
|
XM_011510783.1:c.3317G>A
|
XP_011509085.1:p.Arg1106Lys
|
|
XM_011510784.1:c.3314G>A
|
XP_011509086.1:p.Arg1105Lys
|
|
XM_011510785.1:c.3299G>A
|
XP_011509087.1:p.Arg1100Lys
|
|
XM_011510786.1:c.3194G>A
|
XP_011509088.1:p.Arg1065Lys
|
|
XM_011510787.1:c.3191G>A
|
XP_011509089.1:p.Arg1064Lys
|
|
XM_011510788.1:c.3158G>A
|
XP_011509090.1:p.Arg1053Lys
|
|
XM_011510789.1:c.3008G>A
|
XP_011509091.1:p.Arg1003Lys
|
|
XM_011510790.1:c.2492G>A
|
XP_011509092.1:p.Arg831Lys
|
|
XM_011510791.1:c.2492G>A
|
XP_011509093.1:p.Arg831Lys
|
|
XM_011510792.1:c.3485G>A
|
XP_011509094.1:p.Arg1162Lys
|
|
XR_922888.1:n.3622G>A
|
|
|
XM_011510778.3:c.3485G>A
|
XP_011509080.1:p.Arg1162Lys
|
|
XM_011510779.2:c.3485G>A
|
XP_011509081.1:p.Arg1162Lys
|
|
XM_011510780.2:c.3482G>A
|
XP_011509082.1:p.Arg1161Lys
|
|
XM_011510781.3:c.3467G>A
|
XP_011509083.1:p.Arg1156Lys
|
|
XM_011510782.3:c.3485G>A
|
XP_011509084.1:p.Arg1162Lys
|
|
XM_011510783.3:c.3317G>A
|
XP_011509085.1:p.Arg1106Lys
|
|
XM_011510784.2:c.3314G>A
|
XP_011509086.1:p.Arg1105Lys
|
|
XM_011510785.3:c.3299G>A
|
XP_011509087.1:p.Arg1100Lys
|
|
XM_011510786.3:c.3194G>A
|
XP_011509088.1:p.Arg1065Lys
|
|
XM_011510789.2:c.3008G>A
|
XP_011509091.1:p.Arg1003Lys
|
|
XM_011510792.3:c.3485G>A
|
XP_011509094.1:p.Arg1162Lys
|
|
XM_017003568.1:c.3431G>A
|
XP_016859057.1:p.Arg1144Lys
|
|
XM_017003569.1:c.3263G>A
|
XP_016859058.1:p.Arg1088Lys
|
|
XM_017003570.1:c.2990G>A
|
XP_016859059.1:p.Arg997Lys
|
|
XM_017003571.1:c.2840G>A
|
XP_016859060.1:p.Arg947Lys
|
|
XM_017003572.1:c.2492G>A
|
XP_016859061.1:p.Arg831Lys
|
|
XM_017003573.1:c.2492G>A
|
XP_016859062.1:p.Arg831Lys
|
|
XM_017003574.1:c.2492G>A
|
XP_016859063.1:p.Arg831Lys
|
|
NM_015040.4:c.3449G>A
MANE Select
|
NP_055855.2:p.Arg1150Lys
|
|