ENST00000483750.6:n.790G>T
|
|
|
ENST00000490627.2:n.194G>T
|
|
|
ENST00000698625.1:c.757G>T
|
ENSP00000513844.1:p.Asp253Tyr
|
|
ENST00000698626.1:c.757G>T
|
ENSP00000513845.1:p.Asp253Tyr
|
|
ENST00000698635.1:c.757G>T
|
ENSP00000513850.1:p.Asp253Tyr
|
|
ENST00000376701.5:c.757G>T
MANE Select
|
ENSP00000365891.4:p.Asp253Tyr
|
|
ENST00000376701.4:c.757G>T
|
ENSP00000365891.4:p.Asp253Tyr
|
|
ENST00000465982.5:n.657G>T
|
|
|
ENST00000483750.5:n.783G>T
|
|
|
ENST00000490627.1:n.177G>T
|
|
|
NM_000377.2:c.757G>T , LRG_125t1:c.757G>T
|
NP_000368.1:p.Asp253Tyr
|
|
XM_011543977.1:c.757G>T
|
XP_011542279.1:p.Asp253Tyr
|
|
XM_011543977.2:c.757G>T
|
XP_011542279.1:p.Asp253Tyr
|
|
XM_017029786.1:c.757G>T
|
XP_016885275.1:p.Asp253Tyr
|
|
NM_000377.3:c.757G>T
MANE Select
|
NP_000368.1:p.Asp253Tyr
|
|