ENST00000346342.8:c.858G>A
MANE Select
|
ENSP00000329546.4:p.Leu286=
|
|
ENST00000346342.7:c.858G>A
|
ENSP00000329546.3:p.Leu286=
|
|
ENST00000375581.3:c.924G>A
|
ENSP00000364731.3:p.Leu308=
|
|
ENST00000541084.5:c.672G>A
|
ENSP00000442051.2:p.Leu224=
|
|
NM_000131.4:c.924G>A , LRG_554t1:c.924G>A
|
NP_000122.1:p.Leu308=
|
|
NM_001267554.1:c.672G>A
|
NP_001254483.1:p.Leu224=
|
|
NM_019616.3:c.858G>A , LRG_554t2:c.858G>A
|
NP_062562.1:p.Leu286=
|
|
NR_051961.1:n.945G>A
|
|
|
XM_006719963.2:c.717G>A
|
XP_006720026.1:p.Leu239=
|
|
XM_011537474.1:c.966G>A
|
XP_011535776.1:p.Leu322=
|
|
XM_011537475.1:c.780G>A
|
XP_011535777.1:p.Leu260=
|
|
XM_011537476.1:c.618G>A
|
XP_011535778.1:p.Leu206=
|
|
XM_011537477.1:c.927G>A
|
XP_011535779.1:p.Leu309=
|
|
XM_006719963.3:c.762G>A
|
XP_006720026.2:p.Leu254=
|
|
XM_011537474.2:c.1011G>A
|
XP_011535776.2:p.Leu337=
|
|
XM_011537475.2:c.825G>A
|
XP_011535777.2:p.Leu275=
|
|
XM_011537476.2:c.618G>A
|
XP_011535778.1:p.Leu206=
|
|
NM_019616.4:c.858G>A
MANE Select
|
NP_062562.1:p.Leu286=
|
|
NR_051961.2:n.942G>A
|
|
|
NM_001267554.2:c.672G>A
|
NP_001254483.1:p.Leu224=
|
|