ENST00000299314.12:c.533C=
MANE Select
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ENSP00000299314.7:p.Thr178=
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ENST00000299314.11:c.533C=
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ENSP00000299314.7:p.Thr178=
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ENST00000549940.5:c.533C=
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ENSP00000449150.1:p.Thr178=
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ENST00000550352.1:n.327C=
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|
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ENST00000552681.1:c.167C=
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ENSP00000449217.1:p.Thr56=
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NM_024312.4:c.533C=
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NP_077288.2:p.Thr178=
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XM_006719593.2:c.533C=
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XP_006719656.1:p.Thr178=
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XM_011538731.1:c.452C=
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XP_011537033.1:p.Thr151=
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XM_006719593.3:c.533C=
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XP_006719656.1:p.Thr178=
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XM_011538731.2:c.452C=
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XP_011537033.1:p.Thr151=
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|
XM_017019961.1:c.317C=
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XP_016875450.1:p.Thr106=
|
|
XM_017019962.2:c.-818C=
|
XP_016875451.1:n.-818C=
|
|
NM_024312.5:c.533C=
MANE Select
|
NP_077288.2:p.Thr178=
|
|