ENST00000225927.7:c.1926C=
MANE Select
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ENSP00000225927.1:p.Ser642=
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ENST00000225927.6:c.1926C=
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ENSP00000225927.1:p.Ser642=
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|
ENST00000591587.1:c.1264C=
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ENSP00000467836.1:n.1264C=
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NM_000263.3:c.1926C=
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NP_000254.2:p.Ser642=
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|
XM_006721920.2:c.1095C=
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XP_006721983.1:p.Ser365=
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XM_011524840.1:c.927C=
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XP_011523142.1:p.Ser309=
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|
XM_017024687.1:c.1095C=
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XP_016880176.1:p.Ser365=
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|
XM_024450771.1:c.1983C=
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XP_024306539.1:p.Ser661=
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|
XM_024450772.1:c.927C=
|
XP_024306540.1:p.Ser309=
|
|
NM_000263.4:c.1926C=
MANE Select
|
NP_000254.2:p.Ser642=
|
|