ENST00000268695.10:c.463G>C
MANE Select
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ENSP00000268695.5:p.Gly155Arg
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ENST00000268695.9:c.463G>C
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ENSP00000268695.5:p.Gly155Arg
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ENST00000561812.1:n.419G>C
|
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ENST00000562593.5:n.3872G>C
|
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ENST00000562831.1:c.247G>C
|
ENSP00000455174.1:p.Gly83Arg
|
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ENST00000562931.5:n.51G>C
|
|
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ENST00000566563.1:n.165G>C
|
|
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ENST00000567525.5:c.248-1458G>C
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ENSP00000454484.1:n.248-1458G>C
|
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ENST00000568613.5:c.582G>C
|
ENSP00000457921.1:n.582G>C
|
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NM_000512.4:c.463G>C
|
NP_000503.1:p.Gly155Arg
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XM_005256301.2:c.463G>C
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XP_005256358.1:p.Gly155Arg
|
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XM_005256302.1:c.481G>C
|
XP_005256359.1:p.Gly161Arg
|
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XM_011522982.1:c.481G>C
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XP_011521284.1:p.Gly161Arg
|
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XM_011522984.1:c.481G>C
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XP_011521286.1:p.Gly161Arg
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NM_001323543.1:c.-93G>C
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NP_001310472.1:n.-93G>C
|
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NM_001323544.1:c.481G>C
|
NP_001310473.1:p.Gly161Arg
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XM_005256301.3:c.463G>C
|
XP_005256358.1:p.Gly155Arg
|
|
XM_011522982.2:c.481G>C
|
XP_011521284.1:p.Gly161Arg
|
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XM_017023111.2:c.481G>C
|
XP_016878600.1:p.Gly161Arg
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XM_017023112.2:c.481G>C
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XP_016878601.1:p.Gly161Arg
|
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XM_017023113.1:c.-93G>C
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XP_016878602.1:n.-93G>C
|
|
NM_000512.5:c.463G>C
MANE Select
|
NP_000503.1:p.Gly155Arg
|
|
NM_001323543.2:c.-93G>C
|
NP_001310472.1:n.-93G>C
|
|
NM_001323544.2:c.481G>C
|
NP_001310473.1:p.Gly161Arg
|
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