ENST00000367698.4:c.766C=
MANE Select
|
ENSP00000356671.3:p.Leu256=
|
|
ENST00000367698.3:c.766C=
|
ENSP00000356671.3:p.Leu256=
|
|
ENST00000487183.1:n.417C=
|
|
|
ENST00000617423.4:c.559+1925C=
|
ENSP00000478688.1:n.559+1925C=
|
|
NM_000488.3:c.766C= , LRG_577t1:c.766C=
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NP_000479.1:p.Leu256=
|
|
XM_005245198.2:c.622C=
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XP_005245255.1:p.Leu208=
|
|
NM_001365052.1:c.622C=
|
NP_001351981.1:p.Leu208=
|
|
NM_000488.4:c.766C=
MANE Select
|
NP_000479.1:p.Leu256=
|
|
NM_001365052.2:c.622C=
|
NP_001351981.1:p.Leu208=
|
|
NM_001386302.1:c.889C=
|
NP_001373231.1:p.Leu297=
|
|
NM_001386303.1:c.847C=
|
NP_001373232.1:p.Leu283=
|
|
NM_001386304.1:c.745C=
|
NP_001373233.1:p.Leu249=
|
|
NM_001386305.1:c.763-54C=
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NP_001373234.1:n.763-54C=
|
|
NM_001386306.1:c.550C=
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NP_001373235.1:p.Leu184=
|
|