ENST00000346342.8:c.1309G>A
MANE Select
|
ENSP00000329546.4:p.Val437Ile
|
|
ENST00000346342.7:c.1309G>A
|
ENSP00000329546.3:p.Val437Ile
|
|
ENST00000375581.3:c.1375G>A
|
ENSP00000364731.3:p.Val459Ile
|
|
ENST00000541084.5:c.1123G>A
|
ENSP00000442051.2:p.Val375Ile
|
|
NM_000131.4:c.1375G>A , LRG_554t1:c.1375G>A
|
NP_000122.1:p.Val459Ile
|
|
NM_001267554.1:c.1123G>A
|
NP_001254483.1:p.Val375Ile
|
|
NM_019616.3:c.1309G>A , LRG_554t2:c.1309G>A
|
NP_062562.1:p.Val437Ile
|
|
NR_051961.1:n.1396G>A
|
|
|
XM_006719963.2:c.1168G>A
|
XP_006720026.1:p.Val390Ile
|
|
XM_011537474.1:c.1417G>A
|
XP_011535776.1:p.Val473Ile
|
|
XM_011537475.1:c.1231G>A
|
XP_011535777.1:p.Val411Ile
|
|
XM_011537476.1:c.1069G>A
|
XP_011535778.1:p.Val357Ile
|
|
XM_011537477.1:c.1378G>A
|
XP_011535779.1:p.Val460Ile
|
|
XM_006719963.3:c.1213G>A
|
XP_006720026.2:p.Val405Ile
|
|
XM_011537474.2:c.1462G>A
|
XP_011535776.2:p.Val488Ile
|
|
XM_011537475.2:c.1276G>A
|
XP_011535777.2:p.Val426Ile
|
|
XM_011537476.2:c.1069G>A
|
XP_011535778.1:p.Val357Ile
|
|
NM_019616.4:c.1309G>A
MANE Select
|
NP_062562.1:p.Val437Ile
|
|
NR_051961.2:n.1393G>A
|
|
|
NM_001267554.2:c.1123G>A
|
NP_001254483.1:p.Val375Ile
|
|