ENST00000328300.11:c.4049C>A
MANE Select
|
ENSP00000331902.7:p.Ala1350Asp
|
|
ENST00000361603.7:c.4031C>A
|
ENSP00000354505.2:p.Ala1344Asp
|
|
ENST00000510690.2:n.543C>A
|
|
|
ENST00000328300.10:c.4049C>A
|
ENSP00000331902.6:p.Ala1350Asp
|
|
ENST00000361603.6:c.4031C>A
|
ENSP00000354505.2:p.Ala1344Asp
|
|
ENST00000489230.1:n.452C>A
|
|
|
NM_000495.4:c.4031C>A
|
NP_000486.1:p.Ala1344Asp
|
|
NM_033380.2:c.4049C>A
|
NP_203699.1:p.Ala1350Asp
|
|
XM_005262070.2:c.4040C>A
|
XP_005262127.1:p.Ala1347Asp
|
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XM_006724616.2:c.4049C>A
|
XP_006724679.1:p.Ala1350Asp
|
|
XM_011530849.1:c.3725C>A
|
XP_011529151.1:p.Ala1242Asp
|
|
XM_011530851.1:c.1622C>A
|
XP_011529153.1:p.Ala541Asp
|
|
XM_011530849.2:c.4064C>A
|
XP_011529151.2:p.Ala1355Asp
|
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XM_017029259.2:c.4055C>A
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XP_016884748.1:p.Ala1352Asp
|
|
XM_017029260.1:c.4046C>A
|
XP_016884749.1:p.Ala1349Asp
|
|
XM_017029263.2:c.2384C>A
|
XP_016884752.1:p.Ala795Asp
|
|
NM_000495.5:c.4031C>A
|
NP_000486.1:p.Ala1344Asp
|
|
NM_033380.3:c.4049C>A
MANE Select
|
NP_203699.1:p.Ala1350Asp
|
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