ENST00000346342.8:c.1326A>T
MANE Select
|
ENSP00000329546.4:p.Pro442=
|
|
ENST00000346342.7:c.1326A>T
|
ENSP00000329546.3:p.Pro442=
|
|
ENST00000375581.3:c.1392A>T
|
ENSP00000364731.3:p.Pro464=
|
|
ENST00000541084.5:c.1140A>T
|
ENSP00000442051.2:p.Pro380=
|
|
NM_000131.4:c.1392A>T , LRG_554t1:c.1392A>T
|
NP_000122.1:p.Pro464=
|
|
NM_001267554.1:c.1140A>T
|
NP_001254483.1:p.Pro380=
|
|
NM_019616.3:c.1326A>T , LRG_554t2:c.1326A>T
|
NP_062562.1:p.Pro442=
|
|
NR_051961.1:n.1413A>T
|
|
|
XM_006719963.2:c.1185A>T
|
XP_006720026.1:p.Pro395=
|
|
XM_011537474.1:c.1434A>T
|
XP_011535776.1:p.Pro478=
|
|
XM_011537475.1:c.1248A>T
|
XP_011535777.1:p.Pro416=
|
|
XM_011537476.1:c.1086A>T
|
XP_011535778.1:p.Pro362=
|
|
XM_011537477.1:c.1395A>T
|
XP_011535779.1:p.Pro465=
|
|
XM_006719963.3:c.1230A>T
|
XP_006720026.2:p.Pro410=
|
|
XM_011537474.2:c.1479A>T
|
XP_011535776.2:p.Pro493=
|
|
XM_011537475.2:c.1293A>T
|
XP_011535777.2:p.Pro431=
|
|
XM_011537476.2:c.1086A>T
|
XP_011535778.1:p.Pro362=
|
|
NM_019616.4:c.1326A>T
MANE Select
|
NP_062562.1:p.Pro442=
|
|
NR_051961.2:n.1410A>T
|
|
|
NM_001267554.2:c.1140A>T
|
NP_001254483.1:p.Pro380=
|
|