ENST00000328300.11:c.4914T=
MANE Select
|
ENSP00000331902.7:p.Cys1638=
|
|
ENST00000361603.7:c.4896T=
|
ENSP00000354505.2:p.Cys1632=
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|
ENST00000510690.2:n.1408T=
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|
|
ENST00000644079.1:n.1745T=
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|
|
ENST00000328300.10:c.4914T=
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ENSP00000331902.6:p.Cys1638=
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|
ENST00000361603.6:c.4896T=
|
ENSP00000354505.2:p.Cys1632=
|
|
ENST00000504541.1:c.219+438T=
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ENSP00000424845.1:n.219+438T=
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|
ENST00000515658.1:c.325-938T=
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|
|
NM_000495.4:c.4896T=
|
NP_000486.1:p.Cys1632=
|
|
NM_033380.2:c.4914T=
|
NP_203699.1:p.Cys1638=
|
|
XM_005262070.2:c.4905T=
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XP_005262127.1:p.Cys1635=
|
|
XM_006724616.2:c.4914T=
|
XP_006724679.1:p.Cys1638=
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|
XM_011530849.1:c.4590T=
|
XP_011529151.1:p.Cys1530=
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|
XM_011530851.1:c.2487T=
|
XP_011529153.1:p.Cys829=
|
|
XM_011530849.2:c.4929T=
|
XP_011529151.2:p.Cys1643=
|
|
XM_017029259.2:c.4920T=
|
XP_016884748.1:p.Cys1640=
|
|
XM_017029260.1:c.4911T=
|
XP_016884749.1:p.Cys1637=
|
|
XM_017029263.2:c.3249T=
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XP_016884752.1:p.Cys1083=
|
|
NM_000495.5:c.4896T=
|
NP_000486.1:p.Cys1632=
|
|
NM_033380.3:c.4914T=
MANE Select
|
NP_203699.1:p.Cys1638=
|
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