ENST00000225927.7:c.1821C=
MANE Select
|
ENSP00000225927.1:p.Asp607=
|
|
ENST00000225927.6:c.1821C=
|
ENSP00000225927.1:p.Asp607=
|
|
ENST00000591587.1:c.1159C=
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ENSP00000467836.1:n.1159C=
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|
NM_000263.3:c.1821C=
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NP_000254.2:p.Asp607=
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|
XM_006721920.2:c.990C=
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XP_006721983.1:p.Asp330=
|
|
XM_011524840.1:c.822C=
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XP_011523142.1:p.Asp274=
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|
XM_017024687.1:c.990C=
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XP_016880176.1:p.Asp330=
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|
XM_024450771.1:c.1878C=
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XP_024306539.1:p.Asp626=
|
|
XM_024450772.1:c.822C=
|
XP_024306540.1:p.Asp274=
|
|
NM_000263.4:c.1821C=
MANE Select
|
NP_000254.2:p.Asp607=
|
|