ENST00000346342.8:c.1330C>T
MANE Select
|
ENSP00000329546.4:p.Pro444Ser
|
|
ENST00000346342.7:c.1330C>T
|
ENSP00000329546.3:p.Pro444Ser
|
|
ENST00000375581.3:c.1396C>T
|
ENSP00000364731.3:p.Pro466Ser
|
|
ENST00000541084.5:c.1144C>T
|
ENSP00000442051.2:p.Pro382Ser
|
|
NM_000131.4:c.1396C>T , LRG_554t1:c.1396C>T
|
NP_000122.1:p.Pro466Ser
|
|
NM_001267554.1:c.1144C>T
|
NP_001254483.1:p.Pro382Ser
|
|
NM_019616.3:c.1330C>T , LRG_554t2:c.1330C>T
|
NP_062562.1:p.Pro444Ser
|
|
NR_051961.1:n.1417C>T
|
|
|
XM_006719963.2:c.1189C>T
|
XP_006720026.1:p.Pro397Ser
|
|
XM_011537474.1:c.1438C>T
|
XP_011535776.1:p.Pro480Ser
|
|
XM_011537475.1:c.1252C>T
|
XP_011535777.1:p.Pro418Ser
|
|
XM_011537476.1:c.1090C>T
|
XP_011535778.1:p.Pro364Ser
|
|
XM_011537477.1:c.1399C>T
|
XP_011535779.1:p.Pro467Ser
|
|
XM_006719963.3:c.1234C>T
|
XP_006720026.2:p.Pro412Ser
|
|
XM_011537474.2:c.1483C>T
|
XP_011535776.2:p.Pro495Ser
|
|
XM_011537475.2:c.1297C>T
|
XP_011535777.2:p.Pro433Ser
|
|
XM_011537476.2:c.1090C>T
|
XP_011535778.1:p.Pro364Ser
|
|
NM_019616.4:c.1330C>T
MANE Select
|
NP_062562.1:p.Pro444Ser
|
|
NR_051961.2:n.1414C>T
|
|
|
NM_001267554.2:c.1144C>T
|
NP_001254483.1:p.Pro382Ser
|
|