ENST00000477226.6:n.840G>C
|
|
|
ENST00000683013.1:n.754G>C
|
|
|
ENST00000373960.4:c.1366G>C
MANE Select
|
ENSP00000363071.3:p.Gly456Arg
|
|
ENST00000373960.3:c.1366G>C
|
ENSP00000363071.3:p.Gly456Arg
|
|
ENST00000483395.1:n.221G>C
|
|
|
NM_001927.3:c.1366G>C , LRG_380t1:c.1366G>C
|
NP_001918.3:p.Gly456Arg
|
|
NM_001927.4:c.1366G>C
MANE Select
|
NP_001918.3:p.Gly456Arg
|
|
NM_001382708.1:c.1363G>C
|
NP_001369637.1:p.Gly455Arg
|
|
NM_001382709.1:c.934G>C
|
NP_001369638.1:p.Gly312Arg
|
|
NM_001382710.1:c.1297G>C
|
NP_001369639.1:p.Gly433Arg
|
|
NM_001382711.1:c.1345G>C
|
NP_001369640.1:p.Gly449Arg
|
|
NM_001382712.1:c.1366G>C
|
NP_001369641.1:p.Gly456Arg
|
|
NM_001382713.1:c.1096G>C
|
NP_001369642.1:p.Gly366Arg
|
|