ENST00000302850.10:c.3120C>G
MANE Select
|
ENSP00000303830.4:p.Gly1040=
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|
ENST00000302850.9:c.3120C>G
|
ENSP00000303830.4:p.Gly1040=
|
|
ENST00000341500.9:c.3084C>G
|
ENSP00000342838.4:p.Gly1028=
|
|
NM_000208.2:c.3120C>G
|
NP_000199.2:p.Gly1040=
|
|
NM_000208.3:c.3120C>G
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NP_000199.2:p.Gly1040=
|
|
NM_001079817.1:c.3084C>G
|
NP_001073285.1:p.Gly1028=
|
|
NM_001079817.2:c.3084C>G
|
NP_001073285.1:p.Gly1028=
|
|
XM_011527988.1:c.3195C>G
|
XP_011526290.1:p.Gly1065=
|
|
XM_011527989.1:c.3159C>G
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XP_011526291.1:p.Gly1053=
|
|
XM_011527988.2:c.3117C>G
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XP_011526290.2:p.Gly1039=
|
|
XM_011527989.3:c.3081C>G
|
XP_011526291.2:p.Gly1027=
|
|
NM_000208.4:c.3120C>G
MANE Select
|
NP_000199.2:p.Gly1040=
|
|
NM_001079817.3:c.3084C>G
|
NP_001073285.1:p.Gly1028=
|
|