ENST00000477226.6:n.868A>G
|
|
|
ENST00000683013.1:n.782A>G
|
|
|
ENST00000373960.4:c.1394A>G
MANE Select
|
ENSP00000363071.3:p.Gln465Arg
|
|
ENST00000373960.3:c.1394A>G
|
ENSP00000363071.3:p.Gln465Arg
|
|
ENST00000483395.1:n.249A>G
|
|
|
NM_001927.3:c.1394A>G , LRG_380t1:c.1394A>G
|
NP_001918.3:p.Gln465Arg
|
|
NM_001927.4:c.1394A>G
MANE Select
|
NP_001918.3:p.Gln465Arg
|
|
NM_001382708.1:c.1391A>G
|
NP_001369637.1:p.Gln464Arg
|
|
NM_001382709.1:c.962A>G
|
NP_001369638.1:p.Gln321Arg
|
|
NM_001382710.1:c.1325A>G
|
NP_001369639.1:p.Gln442Arg
|
|
NM_001382711.1:c.1373A>G
|
NP_001369640.1:p.Gln458Arg
|
|
NM_001382712.1:c.1371+226A>G
|
NP_001369641.1:n.1371+226A>G
|
|
NM_001382713.1:c.1124A>G
|
NP_001369642.1:p.Gln375Arg
|
|