ENST00000264380.9:c.3486T>C
MANE Select
|
ENSP00000264380.4:p.Ile1162=
|
|
ENST00000264380.8:c.3486T>C
|
ENSP00000264380.4:p.Ile1162=
|
|
ENST00000452564.1:c.3318T>C
|
ENSP00000405736.1:p.Ile1106=
|
|
NM_015040.3:c.3486T>C
|
NP_055855.2:p.Ile1162=
|
|
XM_011510778.1:c.3522T>C
|
XP_011509080.1:p.Ile1174=
|
|
XM_011510779.1:c.3522T>C
|
XP_011509081.1:p.Ile1174=
|
|
XM_011510780.1:c.3519T>C
|
XP_011509082.1:p.Ile1173=
|
|
XM_011510781.1:c.3504T>C
|
XP_011509083.1:p.Ile1168=
|
|
XM_011510782.1:c.3522T>C
|
XP_011509084.1:p.Ile1174=
|
|
XM_011510783.1:c.3354T>C
|
XP_011509085.1:p.Ile1118=
|
|
XM_011510784.1:c.3351T>C
|
XP_011509086.1:p.Ile1117=
|
|
XM_011510785.1:c.3336T>C
|
XP_011509087.1:p.Ile1112=
|
|
XM_011510786.1:c.3231T>C
|
XP_011509088.1:p.Ile1077=
|
|
XM_011510787.1:c.3228T>C
|
XP_011509089.1:p.Ile1076=
|
|
XM_011510788.1:c.3195T>C
|
XP_011509090.1:p.Ile1065=
|
|
XM_011510789.1:c.3045T>C
|
XP_011509091.1:p.Ile1015=
|
|
XM_011510790.1:c.2529T>C
|
XP_011509092.1:p.Ile843=
|
|
XM_011510791.1:c.2529T>C
|
XP_011509093.1:p.Ile843=
|
|
XM_011510792.1:c.3522T>C
|
XP_011509094.1:p.Ile1174=
|
|
XR_922888.1:n.3659T>C
|
|
|
XM_011510778.3:c.3522T>C
|
XP_011509080.1:p.Ile1174=
|
|
XM_011510779.2:c.3522T>C
|
XP_011509081.1:p.Ile1174=
|
|
XM_011510780.2:c.3519T>C
|
XP_011509082.1:p.Ile1173=
|
|
XM_011510781.3:c.3504T>C
|
XP_011509083.1:p.Ile1168=
|
|
XM_011510782.3:c.3522T>C
|
XP_011509084.1:p.Ile1174=
|
|
XM_011510783.3:c.3354T>C
|
XP_011509085.1:p.Ile1118=
|
|
XM_011510784.2:c.3351T>C
|
XP_011509086.1:p.Ile1117=
|
|
XM_011510785.3:c.3336T>C
|
XP_011509087.1:p.Ile1112=
|
|
XM_011510786.3:c.3231T>C
|
XP_011509088.1:p.Ile1077=
|
|
XM_011510789.2:c.3045T>C
|
XP_011509091.1:p.Ile1015=
|
|
XM_011510792.3:c.3522T>C
|
XP_011509094.1:p.Ile1174=
|
|
XM_017003568.1:c.3468T>C
|
XP_016859057.1:p.Ile1156=
|
|
XM_017003569.1:c.3300T>C
|
XP_016859058.1:p.Ile1100=
|
|
XM_017003570.1:c.3027T>C
|
XP_016859059.1:p.Ile1009=
|
|
XM_017003571.1:c.2877T>C
|
XP_016859060.1:p.Ile959=
|
|
XM_017003572.1:c.2529T>C
|
XP_016859061.1:p.Ile843=
|
|
XM_017003573.1:c.2529T>C
|
XP_016859062.1:p.Ile843=
|
|
XM_017003574.1:c.2529T>C
|
XP_016859063.1:p.Ile843=
|
|
NM_015040.4:c.3486T>C
MANE Select
|
NP_055855.2:p.Ile1162=
|
|