ENST00000346342.8:c.938T>A
MANE Select
|
ENSP00000329546.4:p.Phe313Tyr
|
|
ENST00000346342.7:c.938T>A
|
ENSP00000329546.3:p.Phe313Tyr
|
|
ENST00000375581.3:c.1004T>A
|
ENSP00000364731.3:p.Phe335Tyr
|
|
ENST00000541084.5:c.752T>A
|
ENSP00000442051.2:p.Phe251Tyr
|
|
NM_000131.4:c.1004T>A , LRG_554t1:c.1004T>A
|
NP_000122.1:p.Phe335Tyr
|
|
NM_001267554.1:c.752T>A
|
NP_001254483.1:p.Phe251Tyr
|
|
NM_019616.3:c.938T>A , LRG_554t2:c.938T>A
|
NP_062562.1:p.Phe313Tyr
|
|
NR_051961.1:n.1025T>A
|
|
|
XM_006719963.2:c.797T>A
|
XP_006720026.1:p.Phe266Tyr
|
|
XM_011537474.1:c.1046T>A
|
XP_011535776.1:p.Phe349Tyr
|
|
XM_011537475.1:c.860T>A
|
XP_011535777.1:p.Phe287Tyr
|
|
XM_011537476.1:c.698T>A
|
XP_011535778.1:p.Phe233Tyr
|
|
XM_011537477.1:c.1007T>A
|
XP_011535779.1:p.Phe336Tyr
|
|
XM_006719963.3:c.842T>A
|
XP_006720026.2:p.Phe281Tyr
|
|
XM_011537474.2:c.1091T>A
|
XP_011535776.2:p.Phe364Tyr
|
|
XM_011537475.2:c.905T>A
|
XP_011535777.2:p.Phe302Tyr
|
|
XM_011537476.2:c.698T>A
|
XP_011535778.1:p.Phe233Tyr
|
|
NM_019616.4:c.938T>A
MANE Select
|
NP_062562.1:p.Phe313Tyr
|
|
NR_051961.2:n.1022T>A
|
|
|
NM_001267554.2:c.752T>A
|
NP_001254483.1:p.Phe251Tyr
|
|