ENST00000367698.4:c.838T=
MANE Select
|
ENSP00000356671.3:p.Ser280=
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|
ENST00000367698.3:c.838T=
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ENSP00000356671.3:p.Ser280=
|
|
ENST00000487183.1:n.489T=
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|
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ENST00000617423.4:c.559+1997T=
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ENSP00000478688.1:n.559+1997T=
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NM_000488.3:c.838T= , LRG_577t1:c.838T=
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NP_000479.1:p.Ser280=
|
|
XM_005245198.2:c.694T=
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XP_005245255.1:p.Ser232=
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NM_001365052.1:c.694T=
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NP_001351981.1:p.Ser232=
|
|
NM_000488.4:c.838T=
MANE Select
|
NP_000479.1:p.Ser280=
|
|
NM_001365052.2:c.694T=
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NP_001351981.1:p.Ser232=
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|
NM_001386302.1:c.961T=
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NP_001373231.1:p.Ser321=
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NM_001386303.1:c.919T=
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NP_001373232.1:p.Ser307=
|
|
NM_001386304.1:c.817T=
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NP_001373233.1:p.Ser273=
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NM_001386305.1:c.781T=
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NP_001373234.1:p.Ser261=
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NM_001386306.1:c.622T=
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NP_001373235.1:p.Ser208=
|
|