ENST00000328300.11:c.4309C>G
MANE Select
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ENSP00000331902.7:p.Gln1437Glu
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ENST00000361603.7:c.4291C>G
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ENSP00000354505.2:p.Gln1431Glu
|
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ENST00000510690.2:n.803C>G
|
|
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ENST00000328300.10:c.4309C>G
|
ENSP00000331902.6:p.Gln1437Glu
|
|
ENST00000361603.6:c.4291C>G
|
ENSP00000354505.2:p.Gln1431Glu
|
|
ENST00000489230.1:n.712C>G
|
|
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ENST00000515658.1:c.105C>G
|
|
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NM_000495.4:c.4291C>G
|
NP_000486.1:p.Gln1431Glu
|
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NM_033380.2:c.4309C>G
|
NP_203699.1:p.Gln1437Glu
|
|
XM_005262070.2:c.4300C>G
|
XP_005262127.1:p.Gln1434Glu
|
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XM_006724616.2:c.4309C>G
|
XP_006724679.1:p.Gln1437Glu
|
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XM_011530849.1:c.3985C>G
|
XP_011529151.1:p.Gln1329Glu
|
|
XM_011530851.1:c.1882C>G
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XP_011529153.1:p.Gln628Glu
|
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XM_011530849.2:c.4324C>G
|
XP_011529151.2:p.Gln1442Glu
|
|
XM_017029259.2:c.4315C>G
|
XP_016884748.1:p.Gln1439Glu
|
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XM_017029260.1:c.4306C>G
|
XP_016884749.1:p.Gln1436Glu
|
|
XM_017029263.2:c.2644C>G
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XP_016884752.1:p.Gln882Glu
|
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NM_000495.5:c.4291C>G
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NP_000486.1:p.Gln1431Glu
|
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NM_033380.3:c.4309C>G
MANE Select
|
NP_203699.1:p.Gln1437Glu
|
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