ENST00000324856.13:c.5308G>C
MANE Select
|
ENSP00000320485.7:p.Gly1770Arg
|
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ENST00000374152.7:c.4159G>C
|
ENSP00000363267.2:p.Gly1387Arg
|
|
ENST00000430799.7:c.4156G>C
|
ENSP00000390317.3:p.Gly1386Arg
|
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ENST00000466382.2:c.725G>C
|
|
|
ENST00000636219.1:c.4162G>C
|
ENSP00000489842.1:p.Gly1388Arg
|
|
ENST00000637788.1:n.1108G>C
|
|
|
ENST00000324856.11:c.5308G>C
|
ENSP00000320485.7:p.Gly1770Arg
|
|
ENST00000374152.6:c.4159G>C
|
ENSP00000363267.2:p.Gly1387Arg
|
|
ENST00000430799.6:c.1997G>C
|
|
|
ENST00000457599.6:c.4657G>C
|
ENSP00000387636.2:p.Gly1553Arg
|
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ENST00000466382.1:c.725G>C
|
|
|
ENST00000532781.1:c.806G>C
|
|
|
NM_006015.4:c.5308G>C , LRG_875t1:c.5308G>C
|
NP_006006.3:p.Gly1770Arg
|
|
NM_139135.2:c.4657G>C
|
NP_624361.1:p.Gly1553Arg
|
|
NM_006015.5:c.5308G>C
|
NP_006006.3:p.Gly1770Arg
|
|
NM_139135.3:c.4657G>C
|
NP_624361.1:p.Gly1553Arg
|
|
NM_006015.6:c.5308G>C
MANE Select
|
NP_006006.3:p.Gly1770Arg
|
|
NM_139135.4:c.4657G>C
|
NP_624361.1:p.Gly1553Arg
|
|