ENST00000359271.4:c.489A>C
MANE Select
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ENSP00000352216.2:p.Gly163=
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ENST00000359271.3:c.489A>C
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ENSP00000352216.2:p.Gly163=
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|
NM_030777.3:c.489A>C
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NP_110404.1:p.Gly163=
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XM_011529060.1:c.552A>C
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XP_011527362.1:p.Gly184=
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|
XM_011529061.1:c.498A>C
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XP_011527363.1:p.Gly166=
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|
XM_011529062.1:c.552A>C
|
XP_011527364.1:p.Gly184=
|
|
XM_011529063.1:c.552A>C
|
XP_011527365.1:p.Gly184=
|
|
XM_011529064.1:c.552A>C
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XP_011527366.1:p.Gly184=
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|
XM_011529065.1:c.552A>C
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XP_011527367.1:p.Gly184=
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|
XR_936641.1:n.688A>C
|
|
|
XM_011529060.2:c.552A>C
|
XP_011527362.1:p.Gly184=
|
|
XM_011529061.2:c.498A>C
|
XP_011527363.1:p.Gly166=
|
|
XM_011529062.2:c.552A>C
|
XP_011527364.1:p.Gly184=
|
|
XM_011529063.2:c.552A>C
|
XP_011527365.1:p.Gly184=
|
|
XM_011529064.2:c.552A>C
|
XP_011527366.1:p.Gly184=
|
|
XM_011529065.2:c.552A>C
|
XP_011527367.1:p.Gly184=
|
|
XM_017028087.2:c.489A>C
|
XP_016883576.1:p.Gly163=
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|
XR_936641.2:n.675A>C
|
|
|
NM_030777.4:c.489A>C
MANE Select
|
NP_110404.1:p.Gly163=
|
|