ENST00000483750.6:n.802G>C
|
|
|
ENST00000490627.2:n.206G>C
|
|
|
ENST00000698625.1:c.769G>C
|
ENSP00000513844.1:p.Gly257Arg
|
|
ENST00000698626.1:c.769G>C
|
ENSP00000513845.1:p.Gly257Arg
|
|
ENST00000698635.1:c.769G>C
|
ENSP00000513850.1:p.Gly257Arg
|
|
ENST00000376701.5:c.769G>C
MANE Select
|
ENSP00000365891.4:p.Gly257Arg
|
|
ENST00000376701.4:c.769G>C
|
ENSP00000365891.4:p.Gly257Arg
|
|
ENST00000465982.5:n.669G>C
|
|
|
ENST00000483750.5:n.795G>C
|
|
|
ENST00000490627.1:n.189G>C
|
|
|
NM_000377.2:c.769G>C , LRG_125t1:c.769G>C
|
NP_000368.1:p.Gly257Arg
|
|
XM_011543977.1:c.769G>C
|
XP_011542279.1:p.Gly257Arg
|
|
XM_011543977.2:c.769G>C
|
XP_011542279.1:p.Gly257Arg
|
|
XM_017029786.1:c.769G>C
|
XP_016885275.1:p.Gly257Arg
|
|
NM_000377.3:c.769G>C
MANE Select
|
NP_000368.1:p.Gly257Arg
|
|