ENST00000302850.10:c.3053T>A
MANE Select
|
ENSP00000303830.4:p.Val1018Glu
|
|
ENST00000302850.9:c.3053T>A
|
ENSP00000303830.4:p.Val1018Glu
|
|
ENST00000341500.9:c.3017T>A
|
ENSP00000342838.4:p.Val1006Glu
|
|
NM_000208.2:c.3053T>A
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NP_000199.2:p.Val1018Glu
|
|
NM_000208.3:c.3053T>A
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NP_000199.2:p.Val1018Glu
|
|
NM_001079817.1:c.3017T>A
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NP_001073285.1:p.Val1006Glu
|
|
NM_001079817.2:c.3017T>A
|
NP_001073285.1:p.Val1006Glu
|
|
XM_011527988.1:c.3128T>A
|
XP_011526290.1:p.Val1043Glu
|
|
XM_011527989.1:c.3092T>A
|
XP_011526291.1:p.Val1031Glu
|
|
XM_011527988.2:c.3050T>A
|
XP_011526290.2:p.Val1017Glu
|
|
XM_011527989.3:c.3014T>A
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XP_011526291.2:p.Val1005Glu
|
|
NM_000208.4:c.3053T>A
MANE Select
|
NP_000199.2:p.Val1018Glu
|
|
NM_001079817.3:c.3017T>A
|
NP_001073285.1:p.Val1006Glu
|
|