ENST00000346342.8:c.1163C>T
MANE Select
|
ENSP00000329546.4:p.Thr388Ile
|
|
ENST00000346342.7:c.1163C>T
|
ENSP00000329546.3:p.Thr388Ile
|
|
ENST00000375581.3:c.1229C>T
|
ENSP00000364731.3:p.Thr410Ile
|
|
ENST00000541084.5:c.977C>T
|
ENSP00000442051.2:p.Thr326Ile
|
|
NM_000131.4:c.1229C>T , LRG_554t1:c.1229C>T
|
NP_000122.1:p.Thr410Ile
|
|
NM_001267554.1:c.977C>T
|
NP_001254483.1:p.Thr326Ile
|
|
NM_019616.3:c.1163C>T , LRG_554t2:c.1163C>T
|
NP_062562.1:p.Thr388Ile
|
|
NR_051961.1:n.1250C>T
|
|
|
XM_006719963.2:c.1022C>T
|
XP_006720026.1:p.Thr341Ile
|
|
XM_011537474.1:c.1271C>T
|
XP_011535776.1:p.Thr424Ile
|
|
XM_011537475.1:c.1085C>T
|
XP_011535777.1:p.Thr362Ile
|
|
XM_011537476.1:c.923C>T
|
XP_011535778.1:p.Thr308Ile
|
|
XM_011537477.1:c.1232C>T
|
XP_011535779.1:p.Thr411Ile
|
|
XM_006719963.3:c.1067C>T
|
XP_006720026.2:p.Thr356Ile
|
|
XM_011537474.2:c.1316C>T
|
XP_011535776.2:p.Thr439Ile
|
|
XM_011537475.2:c.1130C>T
|
XP_011535777.2:p.Thr377Ile
|
|
XM_011537476.2:c.923C>T
|
XP_011535778.1:p.Thr308Ile
|
|
NM_019616.4:c.1163C>T
MANE Select
|
NP_062562.1:p.Thr388Ile
|
|
NR_051961.2:n.1247C>T
|
|
|
NM_001267554.2:c.977C>T
|
NP_001254483.1:p.Thr326Ile
|
|