ENST00000346342.8:c.1335G>C
MANE Select
|
ENSP00000329546.4:p.Ter445Tyr
|
|
ENST00000346342.7:c.1335G>C
|
ENSP00000329546.3:p.Ter445Tyr
|
|
ENST00000375581.3:c.1401G>C
|
ENSP00000364731.3:p.Ter467Tyr
|
|
ENST00000541084.5:c.1149G>C
|
ENSP00000442051.2:p.Ter383Tyr
|
|
NM_000131.4:c.1401G>C , LRG_554t1:c.1401G>C
|
NP_000122.1:p.Ter467Tyr
|
|
NM_001267554.1:c.1149G>C
|
NP_001254483.1:p.Ter383Tyr
|
|
NM_019616.3:c.1335G>C , LRG_554t2:c.1335G>C
|
NP_062562.1:p.Ter445Tyr
|
|
NR_051961.1:n.1422G>C
|
|
|
XM_006719963.2:c.1194G>C
|
XP_006720026.1:p.Ter398Tyr
|
|
XM_011537474.1:c.1443G>C
|
XP_011535776.1:p.Ter481Tyr
|
|
XM_011537475.1:c.1257G>C
|
XP_011535777.1:p.Ter419Tyr
|
|
XM_011537476.1:c.1095G>C
|
XP_011535778.1:p.Ter365Tyr
|
|
XM_011537477.1:c.1404G>C
|
XP_011535779.1:p.Ter468Tyr
|
|
XM_006719963.3:c.1239G>C
|
XP_006720026.2:p.Ter413Tyr
|
|
XM_011537474.2:c.1488G>C
|
XP_011535776.2:p.Ter496Tyr
|
|
XM_011537475.2:c.1302G>C
|
XP_011535777.2:p.Ter434Tyr
|
|
XM_011537476.2:c.1095G>C
|
XP_011535778.1:p.Ter365Tyr
|
|
NM_019616.4:c.1335G>C
MANE Select
|
NP_062562.1:p.Ter445Tyr
|
|
NR_051961.2:n.1419G>C
|
|
|
NM_001267554.2:c.1149G>C
|
NP_001254483.1:p.Ter383Tyr
|
|