ENST00000299314.12:c.3147T>A
MANE Select
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ENSP00000299314.7:p.Gly1049=
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ENST00000299314.11:c.3147T>A
|
ENSP00000299314.7:p.Gly1049=
|
|
ENST00000549194.1:n.13T>A
|
|
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NM_024312.4:c.3147T>A
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NP_077288.2:p.Gly1049=
|
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XM_006719593.2:c.3147T>A
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XP_006719656.1:p.Gly1049=
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|
XM_011538731.1:c.3066T>A
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XP_011537033.1:p.Gly1022=
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XM_006719593.3:c.3147T>A
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XP_006719656.1:p.Gly1049=
|
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XM_011538731.2:c.3066T>A
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XP_011537033.1:p.Gly1022=
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XM_017019961.1:c.2931T>A
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XP_016875450.1:p.Gly977=
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XM_017019962.2:c.1920T>A
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XP_016875451.1:p.Gly640=
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NM_024312.5:c.3147T>A
MANE Select
|
NP_077288.2:p.Gly1049=
|
|