ENST00000477226.6:n.776G>C
|
|
|
ENST00000683013.1:n.690G>C
|
|
|
ENST00000373960.4:c.1302G>C
MANE Select
|
ENSP00000363071.3:p.Glu434Asp
|
|
ENST00000373960.3:c.1302G>C
|
ENSP00000363071.3:p.Glu434Asp
|
|
ENST00000483395.1:n.157G>C
|
|
|
NM_001927.3:c.1302G>C , LRG_380t1:c.1302G>C
|
NP_001918.3:p.Glu434Asp
|
|
NM_001927.4:c.1302G>C
MANE Select
|
NP_001918.3:p.Glu434Asp
|
|
NM_001382708.1:c.1299G>C
|
NP_001369637.1:p.Glu433Asp
|
|
NM_001382709.1:c.870G>C
|
NP_001369638.1:p.Glu290Asp
|
|
NM_001382710.1:c.1233G>C
|
NP_001369639.1:p.Glu411Asp
|
|
NM_001382711.1:c.1281G>C
|
NP_001369640.1:p.Glu427Asp
|
|
NM_001382712.1:c.1302G>C
|
NP_001369641.1:p.Glu434Asp
|
|
NM_001382713.1:c.1032G>C
|
NP_001369642.1:p.Glu344Asp
|
|