ENST00000346342.8:c.1311C>T
MANE Select
|
ENSP00000329546.4:p.Val437=
|
|
ENST00000346342.7:c.1311C>T
|
ENSP00000329546.3:p.Val437=
|
|
ENST00000375581.3:c.1377C>T
|
ENSP00000364731.3:p.Val459=
|
|
ENST00000541084.5:c.1125C>T
|
ENSP00000442051.2:p.Val375=
|
|
NM_000131.4:c.1377C>T , LRG_554t1:c.1377C>T
|
NP_000122.1:p.Val459=
|
|
NM_001267554.1:c.1125C>T
|
NP_001254483.1:p.Val375=
|
|
NM_019616.3:c.1311C>T , LRG_554t2:c.1311C>T
|
NP_062562.1:p.Val437=
|
|
NR_051961.1:n.1398C>T
|
|
|
XM_006719963.2:c.1170C>T
|
XP_006720026.1:p.Val390=
|
|
XM_011537474.1:c.1419C>T
|
XP_011535776.1:p.Val473=
|
|
XM_011537475.1:c.1233C>T
|
XP_011535777.1:p.Val411=
|
|
XM_011537476.1:c.1071C>T
|
XP_011535778.1:p.Val357=
|
|
XM_011537477.1:c.1380C>T
|
XP_011535779.1:p.Val460=
|
|
XM_006719963.3:c.1215C>T
|
XP_006720026.2:p.Val405=
|
|
XM_011537474.2:c.1464C>T
|
XP_011535776.2:p.Val488=
|
|
XM_011537475.2:c.1278C>T
|
XP_011535777.2:p.Val426=
|
|
XM_011537476.2:c.1071C>T
|
XP_011535778.1:p.Val357=
|
|
NM_019616.4:c.1311C>T
MANE Select
|
NP_062562.1:p.Val437=
|
|
NR_051961.2:n.1395C>T
|
|
|
NM_001267554.2:c.1125C>T
|
NP_001254483.1:p.Val375=
|
|