ENST00000346342.8:c.1320A>T
MANE Select
|
ENSP00000329546.4:p.Arg440=
|
|
ENST00000346342.7:c.1320A>T
|
ENSP00000329546.3:p.Arg440=
|
|
ENST00000375581.3:c.1386A>T
|
ENSP00000364731.3:p.Arg462=
|
|
ENST00000541084.5:c.1134A>T
|
ENSP00000442051.2:p.Arg378=
|
|
NM_000131.4:c.1386A>T , LRG_554t1:c.1386A>T
|
NP_000122.1:p.Arg462=
|
|
NM_001267554.1:c.1134A>T
|
NP_001254483.1:p.Arg378=
|
|
NM_019616.3:c.1320A>T , LRG_554t2:c.1320A>T
|
NP_062562.1:p.Arg440=
|
|
NR_051961.1:n.1407A>T
|
|
|
XM_006719963.2:c.1179A>T
|
XP_006720026.1:p.Arg393=
|
|
XM_011537474.1:c.1428A>T
|
XP_011535776.1:p.Arg476=
|
|
XM_011537475.1:c.1242A>T
|
XP_011535777.1:p.Arg414=
|
|
XM_011537476.1:c.1080A>T
|
XP_011535778.1:p.Arg360=
|
|
XM_011537477.1:c.1389A>T
|
XP_011535779.1:p.Arg463=
|
|
XM_006719963.3:c.1224A>T
|
XP_006720026.2:p.Arg408=
|
|
XM_011537474.2:c.1473A>T
|
XP_011535776.2:p.Arg491=
|
|
XM_011537475.2:c.1287A>T
|
XP_011535777.2:p.Arg429=
|
|
XM_011537476.2:c.1080A>T
|
XP_011535778.1:p.Arg360=
|
|
NM_019616.4:c.1320A>T
MANE Select
|
NP_062562.1:p.Arg440=
|
|
NR_051961.2:n.1404A>T
|
|
|
NM_001267554.2:c.1134A>T
|
NP_001254483.1:p.Arg378=
|
|