ENST00000225927.7:c.1892G=
MANE Select
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ENSP00000225927.1:p.Ser631=
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ENST00000225927.6:c.1892G=
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ENSP00000225927.1:p.Ser631=
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ENST00000591587.1:c.1230G=
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ENSP00000467836.1:n.1230G=
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NM_000263.3:c.1892G=
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NP_000254.2:p.Ser631=
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XM_006721920.2:c.1061G=
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XP_006721983.1:p.Ser354=
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XM_011524840.1:c.893G=
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XP_011523142.1:p.Ser298=
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XM_017024687.1:c.1061G=
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XP_016880176.1:p.Ser354=
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XM_024450771.1:c.1949G=
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XP_024306539.1:p.Ser650=
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|
XM_024450772.1:c.893G=
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XP_024306540.1:p.Ser298=
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|
NM_000263.4:c.1892G=
MANE Select
|
NP_000254.2:p.Ser631=
|
|