ENST00000477226.6:n.621C>G
|
|
|
ENST00000683013.1:n.535C>G
|
|
|
ENST00000373960.4:c.1147C>G
MANE Select
|
ENSP00000363071.3:p.Arg383Gly
|
|
ENST00000373960.3:c.1147C>G
|
ENSP00000363071.3:p.Arg383Gly
|
|
ENST00000477226.5:n.619C>G
|
|
|
ENST00000492726.1:n.542C>G
|
|
|
NM_001927.3:c.1147C>G , LRG_380t1:c.1147C>G
|
NP_001918.3:p.Arg383Gly
|
|
NM_001927.4:c.1147C>G
MANE Select
|
NP_001918.3:p.Arg383Gly
|
|
NM_001382708.1:c.1144C>G
|
NP_001369637.1:p.Arg382Gly
|
|
NM_001382709.1:c.736-21C>G
|
NP_001369638.1:n.736-21C>G
|
|
NM_001382710.1:c.1078C>G
|
NP_001369639.1:p.Arg360Gly
|
|
NM_001382711.1:c.1126C>G
|
NP_001369640.1:p.Arg376Gly
|
|
NM_001382712.1:c.1147C>G
|
NP_001369641.1:p.Arg383Gly
|
|
NM_001382713.1:c.877C>G
|
NP_001369642.1:p.Arg293Gly
|
|