ENST00000346342.8:c.983G>A
MANE Select
|
ENSP00000329546.4:p.Arg328His
|
|
ENST00000346342.7:c.983G>A
|
ENSP00000329546.3:p.Arg328His
|
|
ENST00000375581.3:c.1049G>A
|
ENSP00000364731.3:p.Arg350His
|
|
ENST00000541084.5:c.797G>A
|
ENSP00000442051.2:p.Arg266His
|
|
NM_000131.4:c.1049G>A , LRG_554t1:c.1049G>A
|
NP_000122.1:p.Arg350His
|
|
NM_001267554.1:c.797G>A
|
NP_001254483.1:p.Arg266His
|
|
NM_019616.3:c.983G>A , LRG_554t2:c.983G>A
|
NP_062562.1:p.Arg328His
|
|
NR_051961.1:n.1070G>A
|
|
|
XM_006719963.2:c.842G>A
|
XP_006720026.1:p.Arg281His
|
|
XM_011537474.1:c.1091G>A
|
XP_011535776.1:p.Arg364His
|
|
XM_011537475.1:c.905G>A
|
XP_011535777.1:p.Arg302His
|
|
XM_011537476.1:c.743G>A
|
XP_011535778.1:p.Arg248His
|
|
XM_011537477.1:c.1052G>A
|
XP_011535779.1:p.Arg351His
|
|
XM_006719963.3:c.887G>A
|
XP_006720026.2:p.Arg296His
|
|
XM_011537474.2:c.1136G>A
|
XP_011535776.2:p.Arg379His
|
|
XM_011537475.2:c.950G>A
|
XP_011535777.2:p.Arg317His
|
|
XM_011537476.2:c.743G>A
|
XP_011535778.1:p.Arg248His
|
|
NM_019616.4:c.983G>A
MANE Select
|
NP_062562.1:p.Arg328His
|
|
NR_051961.2:n.1067G>A
|
|
|
NM_001267554.2:c.797G>A
|
NP_001254483.1:p.Arg266His
|
|