ENST00000302850.10:c.3902T>C
MANE Select
|
ENSP00000303830.4:p.Val1301Ala
|
|
ENST00000302850.9:c.3902T>C
|
ENSP00000303830.4:p.Val1301Ala
|
|
ENST00000341500.9:c.3866T>C
|
ENSP00000342838.4:p.Val1289Ala
|
|
NM_000208.2:c.3902T>C
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NP_000199.2:p.Val1301Ala
|
|
NM_000208.3:c.3902T>C
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NP_000199.2:p.Val1301Ala
|
|
NM_001079817.1:c.3866T>C
|
NP_001073285.1:p.Val1289Ala
|
|
NM_001079817.2:c.3866T>C
|
NP_001073285.1:p.Val1289Ala
|
|
XM_011527988.1:c.3977T>C
|
XP_011526290.1:p.Val1326Ala
|
|
XM_011527989.1:c.3941T>C
|
XP_011526291.1:p.Val1314Ala
|
|
XM_011527988.2:c.3899T>C
|
XP_011526290.2:p.Val1300Ala
|
|
XM_011527989.3:c.3863T>C
|
XP_011526291.2:p.Val1288Ala
|
|
NM_000208.4:c.3902T>C
MANE Select
|
NP_000199.2:p.Val1301Ala
|
|
NM_001079817.3:c.3866T>C
|
NP_001073285.1:p.Val1289Ala
|
|