ENST00000346342.8:c.1299A>G
MANE Select
|
ENSP00000329546.4:p.Pro433=
|
|
ENST00000346342.7:c.1299A>G
|
ENSP00000329546.3:p.Pro433=
|
|
ENST00000375581.3:c.1365A>G
|
ENSP00000364731.3:p.Pro455=
|
|
ENST00000541084.5:c.1113A>G
|
ENSP00000442051.2:p.Pro371=
|
|
NM_000131.4:c.1365A>G , LRG_554t1:c.1365A>G
|
NP_000122.1:p.Pro455=
|
|
NM_001267554.1:c.1113A>G
|
NP_001254483.1:p.Pro371=
|
|
NM_019616.3:c.1299A>G , LRG_554t2:c.1299A>G
|
NP_062562.1:p.Pro433=
|
|
NR_051961.1:n.1386A>G
|
|
|
XM_006719963.2:c.1158A>G
|
XP_006720026.1:p.Pro386=
|
|
XM_011537474.1:c.1407A>G
|
XP_011535776.1:p.Pro469=
|
|
XM_011537475.1:c.1221A>G
|
XP_011535777.1:p.Pro407=
|
|
XM_011537476.1:c.1059A>G
|
XP_011535778.1:p.Pro353=
|
|
XM_011537477.1:c.1368A>G
|
XP_011535779.1:p.Pro456=
|
|
XM_006719963.3:c.1203A>G
|
XP_006720026.2:p.Pro401=
|
|
XM_011537474.2:c.1452A>G
|
XP_011535776.2:p.Pro484=
|
|
XM_011537475.2:c.1266A>G
|
XP_011535777.2:p.Pro422=
|
|
XM_011537476.2:c.1059A>G
|
XP_011535778.1:p.Pro353=
|
|
NM_019616.4:c.1299A>G
MANE Select
|
NP_062562.1:p.Pro433=
|
|
NR_051961.2:n.1383A>G
|
|
|
NM_001267554.2:c.1113A>G
|
NP_001254483.1:p.Pro371=
|
|