ENST00000346342.8:c.1070A>C
MANE Select
|
ENSP00000329546.4:p.Asp357Ala
|
|
ENST00000346342.7:c.1070A>C
|
ENSP00000329546.3:p.Asp357Ala
|
|
ENST00000375581.3:c.1136A>C
|
ENSP00000364731.3:p.Asp379Ala
|
|
ENST00000541084.5:c.884A>C
|
ENSP00000442051.2:p.Asp295Ala
|
|
NM_000131.4:c.1136A>C , LRG_554t1:c.1136A>C
|
NP_000122.1:p.Asp379Ala
|
|
NM_001267554.1:c.884A>C
|
NP_001254483.1:p.Asp295Ala
|
|
NM_019616.3:c.1070A>C , LRG_554t2:c.1070A>C
|
NP_062562.1:p.Asp357Ala
|
|
NR_051961.1:n.1157A>C
|
|
|
XM_006719963.2:c.929A>C
|
XP_006720026.1:p.Asp310Ala
|
|
XM_011537474.1:c.1178A>C
|
XP_011535776.1:p.Asp393Ala
|
|
XM_011537475.1:c.992A>C
|
XP_011535777.1:p.Asp331Ala
|
|
XM_011537476.1:c.830A>C
|
XP_011535778.1:p.Asp277Ala
|
|
XM_011537477.1:c.1139A>C
|
XP_011535779.1:p.Asp380Ala
|
|
XM_006719963.3:c.974A>C
|
XP_006720026.2:p.Asp325Ala
|
|
XM_011537474.2:c.1223A>C
|
XP_011535776.2:p.Asp408Ala
|
|
XM_011537475.2:c.1037A>C
|
XP_011535777.2:p.Asp346Ala
|
|
XM_011537476.2:c.830A>C
|
XP_011535778.1:p.Asp277Ala
|
|
NM_019616.4:c.1070A>C
MANE Select
|
NP_062562.1:p.Asp357Ala
|
|
NR_051961.2:n.1154A>C
|
|
|
NM_001267554.2:c.884A>C
|
NP_001254483.1:p.Asp295Ala
|
|