ENST00000346342.8:c.1287G>T
MANE Select
|
ENSP00000329546.4:p.Met429Ile
|
|
ENST00000346342.7:c.1287G>T
|
ENSP00000329546.3:p.Met429Ile
|
|
ENST00000375581.3:c.1353G>T
|
ENSP00000364731.3:p.Met451Ile
|
|
ENST00000541084.5:c.1101G>T
|
ENSP00000442051.2:p.Met367Ile
|
|
NM_000131.4:c.1353G>T , LRG_554t1:c.1353G>T
|
NP_000122.1:p.Met451Ile
|
|
NM_001267554.1:c.1101G>T
|
NP_001254483.1:p.Met367Ile
|
|
NM_019616.3:c.1287G>T , LRG_554t2:c.1287G>T
|
NP_062562.1:p.Met429Ile
|
|
NR_051961.1:n.1374G>T
|
|
|
XM_006719963.2:c.1146G>T
|
XP_006720026.1:p.Met382Ile
|
|
XM_011537474.1:c.1395G>T
|
XP_011535776.1:p.Met465Ile
|
|
XM_011537475.1:c.1209G>T
|
XP_011535777.1:p.Met403Ile
|
|
XM_011537476.1:c.1047G>T
|
XP_011535778.1:p.Met349Ile
|
|
XM_011537477.1:c.1356G>T
|
XP_011535779.1:p.Met452Ile
|
|
XM_006719963.3:c.1191G>T
|
XP_006720026.2:p.Met397Ile
|
|
XM_011537474.2:c.1440G>T
|
XP_011535776.2:p.Met480Ile
|
|
XM_011537475.2:c.1254G>T
|
XP_011535777.2:p.Met418Ile
|
|
XM_011537476.2:c.1047G>T
|
XP_011535778.1:p.Met349Ile
|
|
NM_019616.4:c.1287G>T
MANE Select
|
NP_062562.1:p.Met429Ile
|
|
NR_051961.2:n.1371G>T
|
|
|
NM_001267554.2:c.1101G>T
|
NP_001254483.1:p.Met367Ile
|
|