ENST00000477226.6:n.834C>T
|
|
|
ENST00000683013.1:n.748C>T
|
|
|
ENST00000373960.4:c.1360C>T
MANE Select
|
ENSP00000363071.3:p.Arg454Trp
|
|
ENST00000373960.3:c.1360C>T
|
ENSP00000363071.3:p.Arg454Trp
|
|
ENST00000483395.1:n.215C>T
|
|
|
NM_001927.3:c.1360C>T , LRG_380t1:c.1360C>T
|
NP_001918.3:p.Arg454Trp
|
|
NM_001927.4:c.1360C>T
MANE Select
|
NP_001918.3:p.Arg454Trp
|
|
NM_001382708.1:c.1357C>T
|
NP_001369637.1:p.Arg453Trp
|
|
NM_001382709.1:c.928C>T
|
NP_001369638.1:p.Arg310Trp
|
|
NM_001382710.1:c.1291C>T
|
NP_001369639.1:p.Arg431Trp
|
|
NM_001382711.1:c.1339C>T
|
NP_001369640.1:p.Arg447Trp
|
|
NM_001382712.1:c.1360C>T
|
NP_001369641.1:p.Arg454Trp
|
|
NM_001382713.1:c.1090C>T
|
NP_001369642.1:p.Arg364Trp
|
|