ENST00000346342.8:c.760C>G
MANE Select
|
ENSP00000329546.4:p.His254Asp
|
|
ENST00000346342.7:c.760C>G
|
ENSP00000329546.3:p.His254Asp
|
|
ENST00000375581.3:c.826C>G
|
ENSP00000364731.3:p.His276Asp
|
|
ENST00000541084.5:c.574C>G
|
ENSP00000442051.2:p.His192Asp
|
|
NM_000131.4:c.826C>G , LRG_554t1:c.826C>G
|
NP_000122.1:p.His276Asp
|
|
NM_001267554.1:c.574C>G
|
NP_001254483.1:p.His192Asp
|
|
NM_019616.3:c.760C>G , LRG_554t2:c.760C>G
|
NP_062562.1:p.His254Asp
|
|
NR_051961.1:n.847C>G
|
|
|
XM_006719963.2:c.619C>G
|
XP_006720026.1:p.His207Asp
|
|
XM_011537474.1:c.868C>G
|
XP_011535776.1:p.His290Asp
|
|
XM_011537475.1:c.682C>G
|
XP_011535777.1:p.His228Asp
|
|
XM_011537476.1:c.520C>G
|
XP_011535778.1:p.His174Asp
|
|
XM_011537477.1:c.829C>G
|
XP_011535779.1:p.His277Asp
|
|
XM_006719963.3:c.664C>G
|
XP_006720026.2:p.His222Asp
|
|
XM_011537474.2:c.913C>G
|
XP_011535776.2:p.His305Asp
|
|
XM_011537475.2:c.727C>G
|
XP_011535777.2:p.His243Asp
|
|
XM_011537476.2:c.520C>G
|
XP_011535778.1:p.His174Asp
|
|
NM_019616.4:c.760C>G
MANE Select
|
NP_062562.1:p.His254Asp
|
|
NR_051961.2:n.844C>G
|
|
|
NM_001267554.2:c.574C>G
|
NP_001254483.1:p.His192Asp
|
|