ENST00000346342.8:c.302A>T
MANE Select
|
ENSP00000329546.4:p.Asp101Val
|
|
ENST00000346342.7:c.302A>T
|
ENSP00000329546.3:p.Asp101Val
|
|
ENST00000375581.3:c.368A>T
|
ENSP00000364731.3:p.Asp123Val
|
|
ENST00000444337.1:c.*110A>T
|
ENSP00000387669.1:n.*110A>T
|
|
ENST00000473085.1:n.249A>T
|
|
|
ENST00000479674.1:n.635A>T
|
|
|
ENST00000541084.5:c.116A>T
|
ENSP00000442051.2:p.Asp39Val
|
|
NM_000131.4:c.368A>T , LRG_554t1:c.368A>T
|
NP_000122.1:p.Asp123Val
|
|
NM_001267554.1:c.116A>T
|
NP_001254483.1:p.Asp39Val
|
|
NM_019616.3:c.302A>T , LRG_554t2:c.302A>T
|
NP_062562.1:p.Asp101Val
|
|
NR_051961.1:n.389A>T
|
|
|
XM_006719963.2:c.302A>T
|
XP_006720026.1:p.Asp101Val
|
|
XM_011537474.1:c.302A>T
|
XP_011535776.1:p.Asp101Val
|
|
XM_011537475.1:c.116A>T
|
XP_011535777.1:p.Asp39Val
|
|
XM_011537477.1:c.263A>T
|
XP_011535779.1:p.Asp88Val
|
|
XM_006719963.3:c.347A>T
|
XP_006720026.2:p.Asp116Val
|
|
XM_011537474.2:c.347A>T
|
XP_011535776.2:p.Asp116Val
|
|
XM_011537475.2:c.161A>T
|
XP_011535777.2:p.Asp54Val
|
|
NM_019616.4:c.302A>T
MANE Select
|
NP_062562.1:p.Asp101Val
|
|
NR_051961.2:n.386A>T
|
|
|
NM_001267554.2:c.116A>T
|
NP_001254483.1:p.Asp39Val
|
|