ENST00000264380.9:c.3484A>T
MANE Select
|
ENSP00000264380.4:p.Ile1162Phe
|
|
ENST00000264380.8:c.3484A>T
|
ENSP00000264380.4:p.Ile1162Phe
|
|
ENST00000452564.1:c.3316A>T
|
ENSP00000405736.1:p.Ile1106Phe
|
|
NM_015040.3:c.3484A>T
|
NP_055855.2:p.Ile1162Phe
|
|
XM_011510778.1:c.3520A>T
|
XP_011509080.1:p.Ile1174Phe
|
|
XM_011510779.1:c.3520A>T
|
XP_011509081.1:p.Ile1174Phe
|
|
XM_011510780.1:c.3517A>T
|
XP_011509082.1:p.Ile1173Phe
|
|
XM_011510781.1:c.3502A>T
|
XP_011509083.1:p.Ile1168Phe
|
|
XM_011510782.1:c.3520A>T
|
XP_011509084.1:p.Ile1174Phe
|
|
XM_011510783.1:c.3352A>T
|
XP_011509085.1:p.Ile1118Phe
|
|
XM_011510784.1:c.3349A>T
|
XP_011509086.1:p.Ile1117Phe
|
|
XM_011510785.1:c.3334A>T
|
XP_011509087.1:p.Ile1112Phe
|
|
XM_011510786.1:c.3229A>T
|
XP_011509088.1:p.Ile1077Phe
|
|
XM_011510787.1:c.3226A>T
|
XP_011509089.1:p.Ile1076Phe
|
|
XM_011510788.1:c.3193A>T
|
XP_011509090.1:p.Ile1065Phe
|
|
XM_011510789.1:c.3043A>T
|
XP_011509091.1:p.Ile1015Phe
|
|
XM_011510790.1:c.2527A>T
|
XP_011509092.1:p.Ile843Phe
|
|
XM_011510791.1:c.2527A>T
|
XP_011509093.1:p.Ile843Phe
|
|
XM_011510792.1:c.3520A>T
|
XP_011509094.1:p.Ile1174Phe
|
|
XR_922888.1:n.3657A>T
|
|
|
XM_011510778.3:c.3520A>T
|
XP_011509080.1:p.Ile1174Phe
|
|
XM_011510779.2:c.3520A>T
|
XP_011509081.1:p.Ile1174Phe
|
|
XM_011510780.2:c.3517A>T
|
XP_011509082.1:p.Ile1173Phe
|
|
XM_011510781.3:c.3502A>T
|
XP_011509083.1:p.Ile1168Phe
|
|
XM_011510782.3:c.3520A>T
|
XP_011509084.1:p.Ile1174Phe
|
|
XM_011510783.3:c.3352A>T
|
XP_011509085.1:p.Ile1118Phe
|
|
XM_011510784.2:c.3349A>T
|
XP_011509086.1:p.Ile1117Phe
|
|
XM_011510785.3:c.3334A>T
|
XP_011509087.1:p.Ile1112Phe
|
|
XM_011510786.3:c.3229A>T
|
XP_011509088.1:p.Ile1077Phe
|
|
XM_011510789.2:c.3043A>T
|
XP_011509091.1:p.Ile1015Phe
|
|
XM_011510792.3:c.3520A>T
|
XP_011509094.1:p.Ile1174Phe
|
|
XM_017003568.1:c.3466A>T
|
XP_016859057.1:p.Ile1156Phe
|
|
XM_017003569.1:c.3298A>T
|
XP_016859058.1:p.Ile1100Phe
|
|
XM_017003570.1:c.3025A>T
|
XP_016859059.1:p.Ile1009Phe
|
|
XM_017003571.1:c.2875A>T
|
XP_016859060.1:p.Ile959Phe
|
|
XM_017003572.1:c.2527A>T
|
XP_016859061.1:p.Ile843Phe
|
|
XM_017003573.1:c.2527A>T
|
XP_016859062.1:p.Ile843Phe
|
|
XM_017003574.1:c.2527A>T
|
XP_016859063.1:p.Ile843Phe
|
|
NM_015040.4:c.3484A>T
MANE Select
|
NP_055855.2:p.Ile1162Phe
|
|