ENST00000346342.8:c.1331C>G
MANE Select
|
ENSP00000329546.4:p.Pro444Arg
|
|
ENST00000346342.7:c.1331C>G
|
ENSP00000329546.3:p.Pro444Arg
|
|
ENST00000375581.3:c.1397C>G
|
ENSP00000364731.3:p.Pro466Arg
|
|
ENST00000541084.5:c.1145C>G
|
ENSP00000442051.2:p.Pro382Arg
|
|
NM_000131.4:c.1397C>G , LRG_554t1:c.1397C>G
|
NP_000122.1:p.Pro466Arg
|
|
NM_001267554.1:c.1145C>G
|
NP_001254483.1:p.Pro382Arg
|
|
NM_019616.3:c.1331C>G , LRG_554t2:c.1331C>G
|
NP_062562.1:p.Pro444Arg
|
|
NR_051961.1:n.1418C>G
|
|
|
XM_006719963.2:c.1190C>G
|
XP_006720026.1:p.Pro397Arg
|
|
XM_011537474.1:c.1439C>G
|
XP_011535776.1:p.Pro480Arg
|
|
XM_011537475.1:c.1253C>G
|
XP_011535777.1:p.Pro418Arg
|
|
XM_011537476.1:c.1091C>G
|
XP_011535778.1:p.Pro364Arg
|
|
XM_011537477.1:c.1400C>G
|
XP_011535779.1:p.Pro467Arg
|
|
XM_006719963.3:c.1235C>G
|
XP_006720026.2:p.Pro412Arg
|
|
XM_011537474.2:c.1484C>G
|
XP_011535776.2:p.Pro495Arg
|
|
XM_011537475.2:c.1298C>G
|
XP_011535777.2:p.Pro433Arg
|
|
XM_011537476.2:c.1091C>G
|
XP_011535778.1:p.Pro364Arg
|
|
NM_019616.4:c.1331C>G
MANE Select
|
NP_062562.1:p.Pro444Arg
|
|
NR_051961.2:n.1415C>G
|
|
|
NM_001267554.2:c.1145C>G
|
NP_001254483.1:p.Pro382Arg
|
|