ENST00000346342.8:c.1153C>T
MANE Select
|
ENSP00000329546.4:p.Pro385Ser
|
|
ENST00000346342.7:c.1153C>T
|
ENSP00000329546.3:p.Pro385Ser
|
|
ENST00000375581.3:c.1219C>T
|
ENSP00000364731.3:p.Pro407Ser
|
|
ENST00000541084.5:c.967C>T
|
ENSP00000442051.2:p.Pro323Ser
|
|
NM_000131.4:c.1219C>T , LRG_554t1:c.1219C>T
|
NP_000122.1:p.Pro407Ser
|
|
NM_001267554.1:c.967C>T
|
NP_001254483.1:p.Pro323Ser
|
|
NM_019616.3:c.1153C>T , LRG_554t2:c.1153C>T
|
NP_062562.1:p.Pro385Ser
|
|
NR_051961.1:n.1240C>T
|
|
|
XM_006719963.2:c.1012C>T
|
XP_006720026.1:p.Pro338Ser
|
|
XM_011537474.1:c.1261C>T
|
XP_011535776.1:p.Pro421Ser
|
|
XM_011537475.1:c.1075C>T
|
XP_011535777.1:p.Pro359Ser
|
|
XM_011537476.1:c.913C>T
|
XP_011535778.1:p.Pro305Ser
|
|
XM_011537477.1:c.1222C>T
|
XP_011535779.1:p.Pro408Ser
|
|
XM_006719963.3:c.1057C>T
|
XP_006720026.2:p.Pro353Ser
|
|
XM_011537474.2:c.1306C>T
|
XP_011535776.2:p.Pro436Ser
|
|
XM_011537475.2:c.1120C>T
|
XP_011535777.2:p.Pro374Ser
|
|
XM_011537476.2:c.913C>T
|
XP_011535778.1:p.Pro305Ser
|
|
NM_019616.4:c.1153C>T
MANE Select
|
NP_062562.1:p.Pro385Ser
|
|
NR_051961.2:n.1237C>T
|
|
|
NM_001267554.2:c.967C>T
|
NP_001254483.1:p.Pro323Ser
|
|