ENST00000477226.6:n.299G>C
|
|
|
ENST00000683013.1:n.213G>C
|
|
|
ENST00000373960.4:c.825G>C
MANE Select
|
ENSP00000363071.3:p.Arg275Ser
|
|
ENST00000373960.3:c.825G>C
|
ENSP00000363071.3:p.Arg275Ser
|
|
ENST00000477226.5:n.297G>C
|
|
|
ENST00000492726.1:n.220G>C
|
|
|
NM_001927.3:c.825G>C , LRG_380t1:c.825G>C
|
NP_001918.3:p.Arg275Ser
|
|
NM_001927.4:c.825G>C
MANE Select
|
NP_001918.3:p.Arg275Ser
|
|
NM_001382708.1:c.822G>C
|
NP_001369637.1:p.Arg274Ser
|
|
NM_001382709.1:c.735+238G>C
|
NP_001369638.1:n.735+238G>C
|
|
NM_001382710.1:c.825G>C
|
NP_001369639.1:p.Arg275Ser
|
|
NM_001382711.1:c.825G>C
|
NP_001369640.1:p.Arg275Ser
|
|
NM_001382712.1:c.825G>C
|
NP_001369641.1:p.Arg275Ser
|
|
NM_001382713.1:c.555G>C
|
NP_001369642.1:p.Arg185Ser
|
|