ENST00000346342.8:c.789G>A
MANE Select
|
ENSP00000329546.4:p.Val263=
|
|
ENST00000346342.7:c.789G>A
|
ENSP00000329546.3:p.Val263=
|
|
ENST00000375581.3:c.855G>A
|
ENSP00000364731.3:p.Val285=
|
|
ENST00000541084.5:c.603G>A
|
ENSP00000442051.2:p.Val201=
|
|
NM_000131.4:c.855G>A , LRG_554t1:c.855G>A
|
NP_000122.1:p.Val285=
|
|
NM_001267554.1:c.603G>A
|
NP_001254483.1:p.Val201=
|
|
NM_019616.3:c.789G>A , LRG_554t2:c.789G>A
|
NP_062562.1:p.Val263=
|
|
NR_051961.1:n.876G>A
|
|
|
XM_006719963.2:c.648G>A
|
XP_006720026.1:p.Val216=
|
|
XM_011537474.1:c.897G>A
|
XP_011535776.1:p.Val299=
|
|
XM_011537475.1:c.711G>A
|
XP_011535777.1:p.Val237=
|
|
XM_011537476.1:c.549G>A
|
XP_011535778.1:p.Val183=
|
|
XM_011537477.1:c.858G>A
|
XP_011535779.1:p.Val286=
|
|
XM_006719963.3:c.693G>A
|
XP_006720026.2:p.Val231=
|
|
XM_011537474.2:c.942G>A
|
XP_011535776.2:p.Val314=
|
|
XM_011537475.2:c.756G>A
|
XP_011535777.2:p.Val252=
|
|
XM_011537476.2:c.549G>A
|
XP_011535778.1:p.Val183=
|
|
NM_019616.4:c.789G>A
MANE Select
|
NP_062562.1:p.Val263=
|
|
NR_051961.2:n.873G>A
|
|
|
NM_001267554.2:c.603G>A
|
NP_001254483.1:p.Val201=
|
|