ENST00000324856.13:c.5284G>C
MANE Select
|
ENSP00000320485.7:p.Gly1762Arg
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ENST00000374152.7:c.4135G>C
|
ENSP00000363267.2:p.Gly1379Arg
|
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ENST00000430799.7:c.4132G>C
|
ENSP00000390317.3:p.Gly1378Arg
|
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ENST00000466382.2:c.701G>C
|
|
|
ENST00000636219.1:c.4138G>C
|
ENSP00000489842.1:p.Gly1380Arg
|
|
ENST00000637788.1:n.1084G>C
|
|
|
ENST00000324856.11:c.5284G>C
|
ENSP00000320485.7:p.Gly1762Arg
|
|
ENST00000374152.6:c.4135G>C
|
ENSP00000363267.2:p.Gly1379Arg
|
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ENST00000430799.6:c.1973G>C
|
|
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ENST00000457599.6:c.4633G>C
|
ENSP00000387636.2:p.Gly1545Arg
|
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ENST00000466382.1:c.701G>C
|
|
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ENST00000532781.1:c.782G>C
|
|
|
NM_006015.4:c.5284G>C , LRG_875t1:c.5284G>C
|
NP_006006.3:p.Gly1762Arg
|
|
NM_139135.2:c.4633G>C
|
NP_624361.1:p.Gly1545Arg
|
|
NM_006015.5:c.5284G>C
|
NP_006006.3:p.Gly1762Arg
|
|
NM_139135.3:c.4633G>C
|
NP_624361.1:p.Gly1545Arg
|
|
NM_006015.6:c.5284G>C
MANE Select
|
NP_006006.3:p.Gly1762Arg
|
|
NM_139135.4:c.4633G>C
|
NP_624361.1:p.Gly1545Arg
|
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