ENST00000346342.8:c.1319G>C
MANE Select
|
ENSP00000329546.4:p.Arg440Pro
|
|
ENST00000346342.7:c.1319G>C
|
ENSP00000329546.3:p.Arg440Pro
|
|
ENST00000375581.3:c.1385G>C
|
ENSP00000364731.3:p.Arg462Pro
|
|
ENST00000541084.5:c.1133G>C
|
ENSP00000442051.2:p.Arg378Pro
|
|
NM_000131.4:c.1385G>C , LRG_554t1:c.1385G>C
|
NP_000122.1:p.Arg462Pro
|
|
NM_001267554.1:c.1133G>C
|
NP_001254483.1:p.Arg378Pro
|
|
NM_019616.3:c.1319G>C , LRG_554t2:c.1319G>C
|
NP_062562.1:p.Arg440Pro
|
|
NR_051961.1:n.1406G>C
|
|
|
XM_006719963.2:c.1178G>C
|
XP_006720026.1:p.Arg393Pro
|
|
XM_011537474.1:c.1427G>C
|
XP_011535776.1:p.Arg476Pro
|
|
XM_011537475.1:c.1241G>C
|
XP_011535777.1:p.Arg414Pro
|
|
XM_011537476.1:c.1079G>C
|
XP_011535778.1:p.Arg360Pro
|
|
XM_011537477.1:c.1388G>C
|
XP_011535779.1:p.Arg463Pro
|
|
XM_006719963.3:c.1223G>C
|
XP_006720026.2:p.Arg408Pro
|
|
XM_011537474.2:c.1472G>C
|
XP_011535776.2:p.Arg491Pro
|
|
XM_011537475.2:c.1286G>C
|
XP_011535777.2:p.Arg429Pro
|
|
XM_011537476.2:c.1079G>C
|
XP_011535778.1:p.Arg360Pro
|
|
NM_019616.4:c.1319G>C
MANE Select
|
NP_062562.1:p.Arg440Pro
|
|
NR_051961.2:n.1403G>C
|
|
|
NM_001267554.2:c.1133G>C
|
NP_001254483.1:p.Arg378Pro
|
|