ENST00000303941.4:c.1446C=
MANE Select
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ENSP00000306678.3:p.Ser482=
|
|
ENST00000303941.3:c.1446C=
|
ENSP00000306678.3:p.Ser482=
|
|
NM_178510.1:c.1446C=
|
NP_848605.1:p.Ser482=
|
|
XM_011542736.1:c.1479C=
|
XP_011541038.1:p.Ser493=
|
|
XM_011542737.1:c.1449C=
|
XP_011541039.1:p.Ser483=
|
|
XM_011542738.1:c.1257C=
|
XP_011541040.1:p.Ser419=
|
|
XM_011542736.2:c.1479C=
|
XP_011541038.1:p.Ser493=
|
|
XM_011542737.2:c.1449C=
|
XP_011541039.1:p.Ser483=
|
|
XM_011542738.2:c.1257C=
|
XP_011541040.1:p.Ser419=
|
|
XM_017017475.1:c.1476C=
|
XP_016872964.1:p.Ser492=
|
|
NM_178510.2:c.1446C=
MANE Select
|
NP_848605.1:p.Ser482=
|
|