ENST00000328300.11:c.4850G>A
MANE Select
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ENSP00000331902.7:p.Gly1617Asp
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ENST00000361603.7:c.4832G>A
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ENSP00000354505.2:p.Gly1611Asp
|
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ENST00000510690.2:n.1344G>A
|
|
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ENST00000644079.1:n.1681G>A
|
|
|
ENST00000328300.10:c.4850G>A
|
ENSP00000331902.6:p.Gly1617Asp
|
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ENST00000361603.6:c.4832G>A
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ENSP00000354505.2:p.Gly1611Asp
|
|
ENST00000504541.1:c.219+374G>A
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ENSP00000424845.1:n.219+374G>A
|
|
ENST00000515658.1:c.325-1002G>A
|
|
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NM_000495.4:c.4832G>A
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NP_000486.1:p.Gly1611Asp
|
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NM_033380.2:c.4850G>A
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NP_203699.1:p.Gly1617Asp
|
|
XM_005262070.2:c.4841G>A
|
XP_005262127.1:p.Gly1614Asp
|
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XM_006724616.2:c.4850G>A
|
XP_006724679.1:p.Gly1617Asp
|
|
XM_011530849.1:c.4526G>A
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XP_011529151.1:p.Gly1509Asp
|
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XM_011530851.1:c.2423G>A
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XP_011529153.1:p.Gly808Asp
|
|
XM_011530849.2:c.4865G>A
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XP_011529151.2:p.Gly1622Asp
|
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XM_017029259.2:c.4856G>A
|
XP_016884748.1:p.Gly1619Asp
|
|
XM_017029260.1:c.4847G>A
|
XP_016884749.1:p.Gly1616Asp
|
|
XM_017029263.2:c.3185G>A
|
XP_016884752.1:p.Gly1062Asp
|
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NM_000495.5:c.4832G>A
|
NP_000486.1:p.Gly1611Asp
|
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NM_033380.3:c.4850G>A
MANE Select
|
NP_203699.1:p.Gly1617Asp
|
|