ENST00000346342.8:c.1284C>A
MANE Select
|
ENSP00000329546.4:p.Leu428=
|
|
ENST00000346342.7:c.1284C>A
|
ENSP00000329546.3:p.Leu428=
|
|
ENST00000375581.3:c.1350C>A
|
ENSP00000364731.3:p.Leu450=
|
|
ENST00000541084.5:c.1098C>A
|
ENSP00000442051.2:p.Leu366=
|
|
NM_000131.4:c.1350C>A , LRG_554t1:c.1350C>A
|
NP_000122.1:p.Leu450=
|
|
NM_001267554.1:c.1098C>A
|
NP_001254483.1:p.Leu366=
|
|
NM_019616.3:c.1284C>A , LRG_554t2:c.1284C>A
|
NP_062562.1:p.Leu428=
|
|
NR_051961.1:n.1371C>A
|
|
|
XM_006719963.2:c.1143C>A
|
XP_006720026.1:p.Leu381=
|
|
XM_011537474.1:c.1392C>A
|
XP_011535776.1:p.Leu464=
|
|
XM_011537475.1:c.1206C>A
|
XP_011535777.1:p.Leu402=
|
|
XM_011537476.1:c.1044C>A
|
XP_011535778.1:p.Leu348=
|
|
XM_011537477.1:c.1353C>A
|
XP_011535779.1:p.Leu451=
|
|
XM_006719963.3:c.1188C>A
|
XP_006720026.2:p.Leu396=
|
|
XM_011537474.2:c.1437C>A
|
XP_011535776.2:p.Leu479=
|
|
XM_011537475.2:c.1251C>A
|
XP_011535777.2:p.Leu417=
|
|
XM_011537476.2:c.1044C>A
|
XP_011535778.1:p.Leu348=
|
|
NM_019616.4:c.1284C>A
MANE Select
|
NP_062562.1:p.Leu428=
|
|
NR_051961.2:n.1368C>A
|
|
|
NM_001267554.2:c.1098C>A
|
NP_001254483.1:p.Leu366=
|
|