ENST00000647814.1:c.2688A>G
MANE Select
|
ENSP00000497274.1:p.Glu896=
|
|
ENST00000370449.8:c.2688A>G
|
ENSP00000359478.4:p.Glu896=
|
|
NM_000392.4:c.2688A>G
|
NP_000383.1:p.Glu896=
|
|
XM_006717630.2:c.1992A>G
|
XP_006717693.1:p.Glu664=
|
|
XM_006717631.2:c.*115A>G
|
XP_006717694.1:n.*115A>G
|
|
XM_011539291.1:c.2688A>G
|
XP_011537593.1:p.Glu896=
|
|
XR_945604.1:n.2877A>G
|
|
|
XR_945605.1:n.2879A>G
|
|
|
NM_000392.5:c.2688A>G
MANE Select
|
NP_000383.2:p.Glu896=
|
|
XM_006717630.3:c.1992A>G
|
XP_006717693.1:p.Glu664=
|
|
XM_006717631.4:c.*115A>G
|
XP_006717694.1:n.*115A>G
|
|
XM_011539291.3:c.2688A>G
|
XP_011537593.1:p.Glu896=
|
|
XR_945604.3:n.2931A>G
|
|
|
XR_945605.3:n.2931A>G
|
|
|