ENST00000264380.9:c.3453G>T
MANE Select
|
ENSP00000264380.4:p.Met1151Ile
|
|
ENST00000264380.8:c.3453G>T
|
ENSP00000264380.4:p.Met1151Ile
|
|
ENST00000452564.1:c.3285G>T
|
ENSP00000405736.1:p.Met1095Ile
|
|
NM_015040.3:c.3453G>T
|
NP_055855.2:p.Met1151Ile
|
|
XM_011510778.1:c.3489G>T
|
XP_011509080.1:p.Met1163Ile
|
|
XM_011510779.1:c.3489G>T
|
XP_011509081.1:p.Met1163Ile
|
|
XM_011510780.1:c.3486G>T
|
XP_011509082.1:p.Met1162Ile
|
|
XM_011510781.1:c.3471G>T
|
XP_011509083.1:p.Met1157Ile
|
|
XM_011510782.1:c.3489G>T
|
XP_011509084.1:p.Met1163Ile
|
|
XM_011510783.1:c.3321G>T
|
XP_011509085.1:p.Met1107Ile
|
|
XM_011510784.1:c.3318G>T
|
XP_011509086.1:p.Met1106Ile
|
|
XM_011510785.1:c.3303G>T
|
XP_011509087.1:p.Met1101Ile
|
|
XM_011510786.1:c.3198G>T
|
XP_011509088.1:p.Met1066Ile
|
|
XM_011510787.1:c.3195G>T
|
XP_011509089.1:p.Met1065Ile
|
|
XM_011510788.1:c.3162G>T
|
XP_011509090.1:p.Met1054Ile
|
|
XM_011510789.1:c.3012G>T
|
XP_011509091.1:p.Met1004Ile
|
|
XM_011510790.1:c.2496G>T
|
XP_011509092.1:p.Met832Ile
|
|
XM_011510791.1:c.2496G>T
|
XP_011509093.1:p.Met832Ile
|
|
XM_011510792.1:c.3489G>T
|
XP_011509094.1:p.Met1163Ile
|
|
XR_922888.1:n.3626G>T
|
|
|
XM_011510778.3:c.3489G>T
|
XP_011509080.1:p.Met1163Ile
|
|
XM_011510779.2:c.3489G>T
|
XP_011509081.1:p.Met1163Ile
|
|
XM_011510780.2:c.3486G>T
|
XP_011509082.1:p.Met1162Ile
|
|
XM_011510781.3:c.3471G>T
|
XP_011509083.1:p.Met1157Ile
|
|
XM_011510782.3:c.3489G>T
|
XP_011509084.1:p.Met1163Ile
|
|
XM_011510783.3:c.3321G>T
|
XP_011509085.1:p.Met1107Ile
|
|
XM_011510784.2:c.3318G>T
|
XP_011509086.1:p.Met1106Ile
|
|
XM_011510785.3:c.3303G>T
|
XP_011509087.1:p.Met1101Ile
|
|
XM_011510786.3:c.3198G>T
|
XP_011509088.1:p.Met1066Ile
|
|
XM_011510789.2:c.3012G>T
|
XP_011509091.1:p.Met1004Ile
|
|
XM_011510792.3:c.3489G>T
|
XP_011509094.1:p.Met1163Ile
|
|
XM_017003568.1:c.3435G>T
|
XP_016859057.1:p.Met1145Ile
|
|
XM_017003569.1:c.3267G>T
|
XP_016859058.1:p.Met1089Ile
|
|
XM_017003570.1:c.2994G>T
|
XP_016859059.1:p.Met998Ile
|
|
XM_017003571.1:c.2844G>T
|
XP_016859060.1:p.Met948Ile
|
|
XM_017003572.1:c.2496G>T
|
XP_016859061.1:p.Met832Ile
|
|
XM_017003573.1:c.2496G>T
|
XP_016859062.1:p.Met832Ile
|
|
XM_017003574.1:c.2496G>T
|
XP_016859063.1:p.Met832Ile
|
|
NM_015040.4:c.3453G>T
MANE Select
|
NP_055855.2:p.Met1151Ile
|
|