ENST00000265343.10:c.3411T>C
MANE Select
|
ENSP00000265343.5:p.Asn1137=
|
|
ENST00000265343.9:c.3411T>C
|
ENSP00000265343.5:p.Asn1137=
|
|
NM_014423.3:c.3411T>C
|
NP_055238.1:p.Asn1137=
|
|
XM_005271963.3:c.3411T>C
|
XP_005272020.1:p.Asn1137=
|
|
XM_005271964.3:c.2277T>C
|
XP_005272021.1:p.Asn759=
|
|
XM_006714587.2:c.3324T>C
|
XP_006714650.1:p.Asn1108=
|
|
XM_005271963.5:c.3411T>C
|
XP_005272020.1:p.Asn1137=
|
|
XM_005271964.4:c.2277T>C
|
XP_005272021.1:p.Asn759=
|
|
XM_006714587.4:c.3324T>C
|
XP_006714650.1:p.Asn1108=
|
|
NM_014423.4:c.3411T>C
MANE Select
|
NP_055238.1:p.Asn1137=
|
|