ENST00000299314.12:c.1096A>G
MANE Select
|
ENSP00000299314.7:p.Thr366Ala
|
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ENST00000299314.11:c.1096A>G
|
ENSP00000299314.7:p.Thr366Ala
|
|
ENST00000549940.5:c.1096A>G
|
ENSP00000449150.1:p.Thr366Ala
|
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NM_024312.4:c.1096A>G
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NP_077288.2:p.Thr366Ala
|
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XM_006719593.2:c.1096A>G
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XP_006719656.1:p.Thr366Ala
|
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XM_011538731.1:c.1015A>G
|
XP_011537033.1:p.Thr339Ala
|
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XM_006719593.3:c.1096A>G
|
XP_006719656.1:p.Thr366Ala
|
|
XM_011538731.2:c.1015A>G
|
XP_011537033.1:p.Thr339Ala
|
|
XM_017019961.1:c.880A>G
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XP_016875450.1:p.Thr294Ala
|
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XM_017019962.2:c.-132A>G
|
XP_016875451.1:n.-132A>G
|
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NM_024312.5:c.1096A>G
MANE Select
|
NP_077288.2:p.Thr366Ala
|
|