ENST00000346342.8:c.1332C>G
MANE Select
|
ENSP00000329546.4:p.Pro444=
|
|
ENST00000346342.7:c.1332C>G
|
ENSP00000329546.3:p.Pro444=
|
|
ENST00000375581.3:c.1398C>G
|
ENSP00000364731.3:p.Pro466=
|
|
ENST00000541084.5:c.1146C>G
|
ENSP00000442051.2:p.Pro382=
|
|
NM_000131.4:c.1398C>G , LRG_554t1:c.1398C>G
|
NP_000122.1:p.Pro466=
|
|
NM_001267554.1:c.1146C>G
|
NP_001254483.1:p.Pro382=
|
|
NM_019616.3:c.1332C>G , LRG_554t2:c.1332C>G
|
NP_062562.1:p.Pro444=
|
|
NR_051961.1:n.1419C>G
|
|
|
XM_006719963.2:c.1191C>G
|
XP_006720026.1:p.Pro397=
|
|
XM_011537474.1:c.1440C>G
|
XP_011535776.1:p.Pro480=
|
|
XM_011537475.1:c.1254C>G
|
XP_011535777.1:p.Pro418=
|
|
XM_011537476.1:c.1092C>G
|
XP_011535778.1:p.Pro364=
|
|
XM_011537477.1:c.1401C>G
|
XP_011535779.1:p.Pro467=
|
|
XM_006719963.3:c.1236C>G
|
XP_006720026.2:p.Pro412=
|
|
XM_011537474.2:c.1485C>G
|
XP_011535776.2:p.Pro495=
|
|
XM_011537475.2:c.1299C>G
|
XP_011535777.2:p.Pro433=
|
|
XM_011537476.2:c.1092C>G
|
XP_011535778.1:p.Pro364=
|
|
NM_019616.4:c.1332C>G
MANE Select
|
NP_062562.1:p.Pro444=
|
|
NR_051961.2:n.1416C>G
|
|
|
NM_001267554.2:c.1146C>G
|
NP_001254483.1:p.Pro382=
|
|