ENST00000328300.11:c.4836G>C
MANE Select
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ENSP00000331902.7:p.Gly1612=
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ENST00000361603.7:c.4818G>C
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ENSP00000354505.2:p.Gly1606=
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ENST00000510690.2:n.1330G>C
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ENST00000644079.1:n.1667G>C
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ENST00000328300.10:c.4836G>C
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ENSP00000331902.6:p.Gly1612=
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ENST00000361603.6:c.4818G>C
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ENSP00000354505.2:p.Gly1606=
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ENST00000504541.1:c.219+360G>C
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ENSP00000424845.1:n.219+360G>C
|
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ENST00000515658.1:c.325-1016G>C
|
|
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NM_000495.4:c.4818G>C
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NP_000486.1:p.Gly1606=
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NM_033380.2:c.4836G>C
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NP_203699.1:p.Gly1612=
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XM_005262070.2:c.4827G>C
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XP_005262127.1:p.Gly1609=
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XM_006724616.2:c.4836G>C
|
XP_006724679.1:p.Gly1612=
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XM_011530849.1:c.4512G>C
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XP_011529151.1:p.Gly1504=
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XM_011530851.1:c.2409G>C
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XP_011529153.1:p.Gly803=
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XM_011530849.2:c.4851G>C
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XP_011529151.2:p.Gly1617=
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XM_017029259.2:c.4842G>C
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XP_016884748.1:p.Gly1614=
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XM_017029260.1:c.4833G>C
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XP_016884749.1:p.Gly1611=
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XM_017029263.2:c.3171G>C
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XP_016884752.1:p.Gly1057=
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NM_000495.5:c.4818G>C
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NP_000486.1:p.Gly1606=
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NM_033380.3:c.4836G>C
MANE Select
|
NP_203699.1:p.Gly1612=
|
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