ENST00000346342.8:c.1288C>G
MANE Select
|
ENSP00000329546.4:p.Arg430Gly
|
|
ENST00000346342.7:c.1288C>G
|
ENSP00000329546.3:p.Arg430Gly
|
|
ENST00000375581.3:c.1354C>G
|
ENSP00000364731.3:p.Arg452Gly
|
|
ENST00000541084.5:c.1102C>G
|
ENSP00000442051.2:p.Arg368Gly
|
|
NM_000131.4:c.1354C>G , LRG_554t1:c.1354C>G
|
NP_000122.1:p.Arg452Gly
|
|
NM_001267554.1:c.1102C>G
|
NP_001254483.1:p.Arg368Gly
|
|
NM_019616.3:c.1288C>G , LRG_554t2:c.1288C>G
|
NP_062562.1:p.Arg430Gly
|
|
NR_051961.1:n.1375C>G
|
|
|
XM_006719963.2:c.1147C>G
|
XP_006720026.1:p.Arg383Gly
|
|
XM_011537474.1:c.1396C>G
|
XP_011535776.1:p.Arg466Gly
|
|
XM_011537475.1:c.1210C>G
|
XP_011535777.1:p.Arg404Gly
|
|
XM_011537476.1:c.1048C>G
|
XP_011535778.1:p.Arg350Gly
|
|
XM_011537477.1:c.1357C>G
|
XP_011535779.1:p.Arg453Gly
|
|
XM_006719963.3:c.1192C>G
|
XP_006720026.2:p.Arg398Gly
|
|
XM_011537474.2:c.1441C>G
|
XP_011535776.2:p.Arg481Gly
|
|
XM_011537475.2:c.1255C>G
|
XP_011535777.2:p.Arg419Gly
|
|
XM_011537476.2:c.1048C>G
|
XP_011535778.1:p.Arg350Gly
|
|
NM_019616.4:c.1288C>G
MANE Select
|
NP_062562.1:p.Arg430Gly
|
|
NR_051961.2:n.1372C>G
|
|
|
NM_001267554.2:c.1102C>G
|
NP_001254483.1:p.Arg368Gly
|
|