ENST00000225964.10:c.4182C=
MANE Select
|
ENSP00000225964.6:p.Asn1394=
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|
ENST00000225964.9:c.4182C=
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ENSP00000225964.5:p.Asn1394=
|
|
ENST00000510710.3:n.1147C=
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|
|
NM_000088.3:c.4182C= , LRG_1t1:c.4182C=
|
NP_000079.2:p.Asn1394=
|
|
XM_005257058.3:c.3912C=
|
XP_005257115.2:p.Asn1304=
|
|
XM_005257059.3:c.3264C=
|
XP_005257116.2:p.Asn1088=
|
|
XM_011524341.1:c.3984C=
|
XP_011522643.1:p.Asn1328=
|
|
XM_005257058.4:c.3912C=
|
XP_005257115.2:p.Asn1304=
|
|
XM_005257059.4:c.3264C=
|
XP_005257116.2:p.Asn1088=
|
|
NM_000088.4:c.4182C=
MANE Select
|
NP_000079.2:p.Asn1394=
|
|