ENST00000299314.12:c.3146G>C
MANE Select
|
ENSP00000299314.7:p.Gly1049Ala
|
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ENST00000299314.11:c.3146G>C
|
ENSP00000299314.7:p.Gly1049Ala
|
|
ENST00000549194.1:n.12G>C
|
|
|
NM_024312.4:c.3146G>C
|
NP_077288.2:p.Gly1049Ala
|
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XM_006719593.2:c.3146G>C
|
XP_006719656.1:p.Gly1049Ala
|
|
XM_011538731.1:c.3065G>C
|
XP_011537033.1:p.Gly1022Ala
|
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XM_006719593.3:c.3146G>C
|
XP_006719656.1:p.Gly1049Ala
|
|
XM_011538731.2:c.3065G>C
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XP_011537033.1:p.Gly1022Ala
|
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XM_017019961.1:c.2930G>C
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XP_016875450.1:p.Gly977Ala
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XM_017019962.2:c.1919G>C
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XP_016875451.1:p.Gly640Ala
|
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NM_024312.5:c.3146G>C
MANE Select
|
NP_077288.2:p.Gly1049Ala
|
|