ENST00000346342.8:c.775C>T
MANE Select
|
ENSP00000329546.4:p.Gln259Ter
|
|
ENST00000346342.7:c.775C>T
|
ENSP00000329546.3:p.Gln259Ter
|
|
ENST00000375581.3:c.841C>T
|
ENSP00000364731.3:p.Gln281Ter
|
|
ENST00000541084.5:c.589C>T
|
ENSP00000442051.2:p.Gln197Ter
|
|
NM_000131.4:c.841C>T , LRG_554t1:c.841C>T
|
NP_000122.1:p.Gln281Ter
|
|
NM_001267554.1:c.589C>T
|
NP_001254483.1:p.Gln197Ter
|
|
NM_019616.3:c.775C>T , LRG_554t2:c.775C>T
|
NP_062562.1:p.Gln259Ter
|
|
NR_051961.1:n.862C>T
|
|
|
XM_006719963.2:c.634C>T
|
XP_006720026.1:p.Gln212Ter
|
|
XM_011537474.1:c.883C>T
|
XP_011535776.1:p.Gln295Ter
|
|
XM_011537475.1:c.697C>T
|
XP_011535777.1:p.Gln233Ter
|
|
XM_011537476.1:c.535C>T
|
XP_011535778.1:p.Gln179Ter
|
|
XM_011537477.1:c.844C>T
|
XP_011535779.1:p.Gln282Ter
|
|
XM_006719963.3:c.679C>T
|
XP_006720026.2:p.Gln227Ter
|
|
XM_011537474.2:c.928C>T
|
XP_011535776.2:p.Gln310Ter
|
|
XM_011537475.2:c.742C>T
|
XP_011535777.2:p.Gln248Ter
|
|
XM_011537476.2:c.535C>T
|
XP_011535778.1:p.Gln179Ter
|
|
NM_019616.4:c.775C>T
MANE Select
|
NP_062562.1:p.Gln259Ter
|
|
NR_051961.2:n.859C>T
|
|
|
NM_001267554.2:c.589C>T
|
NP_001254483.1:p.Gln197Ter
|
|