ENST00000346342.8:c.1328T>A
MANE Select
|
ENSP00000329546.4:p.Phe443Tyr
|
|
ENST00000346342.7:c.1328T>A
|
ENSP00000329546.3:p.Phe443Tyr
|
|
ENST00000375581.3:c.1394T>A
|
ENSP00000364731.3:p.Phe465Tyr
|
|
ENST00000541084.5:c.1142T>A
|
ENSP00000442051.2:p.Phe381Tyr
|
|
NM_000131.4:c.1394T>A , LRG_554t1:c.1394T>A
|
NP_000122.1:p.Phe465Tyr
|
|
NM_001267554.1:c.1142T>A
|
NP_001254483.1:p.Phe381Tyr
|
|
NM_019616.3:c.1328T>A , LRG_554t2:c.1328T>A
|
NP_062562.1:p.Phe443Tyr
|
|
NR_051961.1:n.1415T>A
|
|
|
XM_006719963.2:c.1187T>A
|
XP_006720026.1:p.Phe396Tyr
|
|
XM_011537474.1:c.1436T>A
|
XP_011535776.1:p.Phe479Tyr
|
|
XM_011537475.1:c.1250T>A
|
XP_011535777.1:p.Phe417Tyr
|
|
XM_011537476.1:c.1088T>A
|
XP_011535778.1:p.Phe363Tyr
|
|
XM_011537477.1:c.1397T>A
|
XP_011535779.1:p.Phe466Tyr
|
|
XM_006719963.3:c.1232T>A
|
XP_006720026.2:p.Phe411Tyr
|
|
XM_011537474.2:c.1481T>A
|
XP_011535776.2:p.Phe494Tyr
|
|
XM_011537475.2:c.1295T>A
|
XP_011535777.2:p.Phe432Tyr
|
|
XM_011537476.2:c.1088T>A
|
XP_011535778.1:p.Phe363Tyr
|
|
NM_019616.4:c.1328T>A
MANE Select
|
NP_062562.1:p.Phe443Tyr
|
|
NR_051961.2:n.1412T>A
|
|
|
NM_001267554.2:c.1142T>A
|
NP_001254483.1:p.Phe381Tyr
|
|