ENST00000477226.6:n.716C>A
|
|
|
ENST00000683013.1:n.630C>A
|
|
|
ENST00000373960.4:c.1242C>A
MANE Select
|
ENSP00000363071.3:p.Ser414Arg
|
|
ENST00000373960.3:c.1242C>A
|
ENSP00000363071.3:p.Ser414Arg
|
|
ENST00000477226.5:n.714C>A
|
|
|
ENST00000492726.1:n.637C>A
|
|
|
NM_001927.3:c.1242C>A , LRG_380t1:c.1242C>A
|
NP_001918.3:p.Ser414Arg
|
|
NM_001927.4:c.1242C>A
MANE Select
|
NP_001918.3:p.Ser414Arg
|
|
NM_001382708.1:c.1239C>A
|
NP_001369637.1:p.Ser413Arg
|
|
NM_001382709.1:c.810C>A
|
NP_001369638.1:p.Ser270Arg
|
|
NM_001382710.1:c.1173C>A
|
NP_001369639.1:p.Ser391Arg
|
|
NM_001382711.1:c.1221C>A
|
NP_001369640.1:p.Ser407Arg
|
|
NM_001382712.1:c.1242C>A
|
NP_001369641.1:p.Ser414Arg
|
|
NM_001382713.1:c.972C>A
|
NP_001369642.1:p.Ser324Arg
|
|