ENST00000181839.10:c.2052G>T
MANE Select
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ENSP00000181839.4:p.Gly684=
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ENST00000340829.10:c.2052G>T
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ENSP00000340557.5:p.Gly684=
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ENST00000484589.2:c.604G>T
|
|
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ENST00000642213.1:n.534G>T
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|
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ENST00000642660.1:n.932G>T
|
|
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ENST00000643859.1:c.943G>T
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ENST00000643915.1:c.366G>T
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ENSP00000496187.1:p.Gly122=
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ENST00000646039.1:c.1392G>T
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ENSP00000494168.1:p.Gly464=
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ENST00000646437.1:c.686G>T
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|
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ENST00000647453.1:n.1121G>T
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ENST00000647518.1:n.3889G>T
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ENST00000181839.8:c.2052G>T
|
ENSP00000181839.4:p.Gly684=
|
|
ENST00000340829.9:c.2052G>T
|
ENSP00000340557.5:p.Gly684=
|
|
ENST00000484589.1:n.604G>T
|
|
|
ENST00000611390.1:c.210G>T
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ENSP00000484610.1:p.Gly70=
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ENST00000613626.4:c.210G>T
|
ENSP00000480835.1:p.Gly70=
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NM_003718.4:c.2052G>T
|
NP_003709.3:p.Gly684=
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|
NM_031267.3:c.2052G>T
|
NP_112557.2:p.Gly684=
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|
XM_011515597.1:c.2052G>T
|
XP_011513899.1:p.Gly684=
|
|
XM_011515598.1:c.2052G>T
|
XP_011513900.1:p.Gly684=
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|
XM_011515597.3:c.2052G>T
|
XP_011513899.1:p.Gly684=
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XM_017012750.2:c.2052G>T
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XP_016868239.1:p.Gly684=
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XM_017012751.2:c.2052G>T
|
XP_016868240.1:p.Gly684=
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|
NM_003718.5:c.2052G>T
MANE Select
|
NP_003709.3:p.Gly684=
|
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