ENST00000346342.8:c.838G>C
MANE Select
|
ENSP00000329546.4:p.Asp280His
|
|
ENST00000346342.7:c.838G>C
|
ENSP00000329546.3:p.Asp280His
|
|
ENST00000375581.3:c.904G>C
|
ENSP00000364731.3:p.Asp302His
|
|
ENST00000541084.5:c.652G>C
|
ENSP00000442051.2:p.Asp218His
|
|
NM_000131.4:c.904G>C , LRG_554t1:c.904G>C
|
NP_000122.1:p.Asp302His
|
|
NM_001267554.1:c.652G>C
|
NP_001254483.1:p.Asp218His
|
|
NM_019616.3:c.838G>C , LRG_554t2:c.838G>C
|
NP_062562.1:p.Asp280His
|
|
NR_051961.1:n.925G>C
|
|
|
XM_006719963.2:c.697G>C
|
XP_006720026.1:p.Asp233His
|
|
XM_011537474.1:c.946G>C
|
XP_011535776.1:p.Asp316His
|
|
XM_011537475.1:c.760G>C
|
XP_011535777.1:p.Asp254His
|
|
XM_011537476.1:c.598G>C
|
XP_011535778.1:p.Asp200His
|
|
XM_011537477.1:c.907G>C
|
XP_011535779.1:p.Asp303His
|
|
XM_006719963.3:c.742G>C
|
XP_006720026.2:p.Asp248His
|
|
XM_011537474.2:c.991G>C
|
XP_011535776.2:p.Asp331His
|
|
XM_011537475.2:c.805G>C
|
XP_011535777.2:p.Asp269His
|
|
XM_011537476.2:c.598G>C
|
XP_011535778.1:p.Asp200His
|
|
NM_019616.4:c.838G>C
MANE Select
|
NP_062562.1:p.Asp280His
|
|
NR_051961.2:n.922G>C
|
|
|
NM_001267554.2:c.652G>C
|
NP_001254483.1:p.Asp218His
|
|