ENST00000346342.8:c.1298C>G
MANE Select
|
ENSP00000329546.4:p.Pro433Arg
|
|
ENST00000346342.7:c.1298C>G
|
ENSP00000329546.3:p.Pro433Arg
|
|
ENST00000375581.3:c.1364C>G
|
ENSP00000364731.3:p.Pro455Arg
|
|
ENST00000541084.5:c.1112C>G
|
ENSP00000442051.2:p.Pro371Arg
|
|
NM_000131.4:c.1364C>G , LRG_554t1:c.1364C>G
|
NP_000122.1:p.Pro455Arg
|
|
NM_001267554.1:c.1112C>G
|
NP_001254483.1:p.Pro371Arg
|
|
NM_019616.3:c.1298C>G , LRG_554t2:c.1298C>G
|
NP_062562.1:p.Pro433Arg
|
|
NR_051961.1:n.1385C>G
|
|
|
XM_006719963.2:c.1157C>G
|
XP_006720026.1:p.Pro386Arg
|
|
XM_011537474.1:c.1406C>G
|
XP_011535776.1:p.Pro469Arg
|
|
XM_011537475.1:c.1220C>G
|
XP_011535777.1:p.Pro407Arg
|
|
XM_011537476.1:c.1058C>G
|
XP_011535778.1:p.Pro353Arg
|
|
XM_011537477.1:c.1367C>G
|
XP_011535779.1:p.Pro456Arg
|
|
XM_006719963.3:c.1202C>G
|
XP_006720026.2:p.Pro401Arg
|
|
XM_011537474.2:c.1451C>G
|
XP_011535776.2:p.Pro484Arg
|
|
XM_011537475.2:c.1265C>G
|
XP_011535777.2:p.Pro422Arg
|
|
XM_011537476.2:c.1058C>G
|
XP_011535778.1:p.Pro353Arg
|
|
NM_019616.4:c.1298C>G
MANE Select
|
NP_062562.1:p.Pro433Arg
|
|
NR_051961.2:n.1382C>G
|
|
|
NM_001267554.2:c.1112C>G
|
NP_001254483.1:p.Pro371Arg
|
|