ENST00000302850.10:c.3631G>A
MANE Select
|
ENSP00000303830.4:p.Gly1211Arg
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ENST00000302850.9:c.3631G>A
|
ENSP00000303830.4:p.Gly1211Arg
|
|
ENST00000341500.9:c.3595G>A
|
ENSP00000342838.4:p.Gly1199Arg
|
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ENST00000601099.1:n.542G>A
|
|
|
NM_000208.2:c.3631G>A
|
NP_000199.2:p.Gly1211Arg
|
|
NM_000208.3:c.3631G>A
|
NP_000199.2:p.Gly1211Arg
|
|
NM_001079817.1:c.3595G>A
|
NP_001073285.1:p.Gly1199Arg
|
|
NM_001079817.2:c.3595G>A
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NP_001073285.1:p.Gly1199Arg
|
|
XM_011527988.1:c.3706G>A
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XP_011526290.1:p.Gly1236Arg
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XM_011527989.1:c.3670G>A
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XP_011526291.1:p.Gly1224Arg
|
|
XM_011527988.2:c.3628G>A
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XP_011526290.2:p.Gly1210Arg
|
|
XM_011527989.3:c.3592G>A
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XP_011526291.2:p.Gly1198Arg
|
|
NM_000208.4:c.3631G>A
MANE Select
|
NP_000199.2:p.Gly1211Arg
|
|
NM_001079817.3:c.3595G>A
|
NP_001073285.1:p.Gly1199Arg
|
|