ENST00000281928.9:c.5578T>C
MANE Select
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ENSP00000281928.3:p.Leu1860=
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ENST00000548694.2:n.367T>C
|
|
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ENST00000648379.1:n.3946T>C
|
|
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ENST00000648737.1:n.5342T>C
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|
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ENST00000648825.1:n.3763T>C
|
|
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ENST00000648916.1:n.3589T>C
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|
|
ENST00000649607.1:c.3762T>C
|
|
|
ENST00000649775.1:c.2067T>C
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|
|
ENST00000650226.1:c.5578T>C
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ENSP00000496981.1:p.Leu1860=
|
|
ENST00000281928.7:c.5578T>C
|
ENSP00000281928.3:p.Leu1860=
|
|
ENST00000548694.1:n.367T>C
|
|
|
ENST00000552447.1:c.155T>C
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|
|
NM_015335.4:c.5578T>C
|
NP_056150.1:p.Leu1860=
|
|
XM_011538080.1:c.5578T>C
|
XP_011536382.1:p.Leu1860=
|
|
XM_011538081.1:c.5575T>C
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XP_011536383.1:p.Leu1859=
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XM_011538082.1:c.5548T>C
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XP_011536384.1:p.Leu1850=
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|
XM_011538080.2:c.5578T>C
|
XP_011536382.1:p.Leu1860=
|
|
XM_011538081.2:c.5575T>C
|
XP_011536383.1:p.Leu1859=
|
|
XM_011538082.2:c.5548T>C
|
XP_011536384.1:p.Leu1850=
|
|
XM_017019090.1:c.5575T>C
|
XP_016874579.1:p.Leu1859=
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|
NM_015335.5:c.5578T>C
MANE Select
|
NP_056150.1:p.Leu1860=
|
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