ENST00000222747.8:c.415G>T
MANE Select
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ENSP00000222747.3:p.Gly139Ter
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ENST00000222747.7:c.415G>T
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ENSP00000222747.3:p.Gly139Ter
|
|
ENST00000415871.5:c.415G>T
|
ENSP00000397699.1:p.Gly139Ter
|
|
ENST00000441017.5:c.415G>T
|
ENSP00000411158.1:p.Gly139Ter
|
|
ENST00000450414.5:c.394G>T
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ENSP00000397411.1:n.394G>T
|
|
NM_012338.3:c.415G>T
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NP_036470.1:p.Gly139Ter
|
|
XM_005250239.1:c.415G>T
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XP_005250296.1:p.Gly139Ter
|
|
XM_011515993.1:c.415G>T
|
XP_011514295.1:p.Gly139Ter
|
|
XM_011515994.1:c.415G>T
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XP_011514296.1:p.Gly139Ter
|
|
XM_005250239.3:c.415G>T
|
XP_005250296.1:p.Gly139Ter
|
|
XM_017011913.1:c.340G>T
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XP_016867402.1:p.Gly114Ter
|
|
NM_012338.4:c.415G>T
MANE Select
|
NP_036470.1:p.Gly139Ter
|
|