ENST00000647814.1:c.2629_2630insACTA
MANE Select
|
ENSP00000497274.1:p.Gly877AspfsTer2
|
|
ENST00000370449.8:c.2629_2630insACTA
|
ENSP00000359478.4:p.Gly877AspfsTer2
|
|
NM_000392.4:c.2629_2630insACTA
|
NP_000383.1:p.Gly877AspfsTer2
|
|
XM_006717630.2:c.1933_1934insACTA
|
XP_006717693.1:p.Gly645AspfsTer2
|
|
XM_006717631.2:c.*56_*57insACTA
|
XP_006717694.1:n.*56_*57insACTA
|
|
XM_011539291.1:c.2629_2630insACTA
|
XP_011537593.1:p.Gly877AspfsTer2
|
|
XR_945604.1:n.2818_2819insACTA
|
|
|
XR_945605.1:n.2820_2821insACTA
|
|
|
NM_000392.5:c.2629_2630insACTA
MANE Select
|
NP_000383.2:p.Gly877AspfsTer2
|
|
XM_006717630.3:c.1933_1934insACTA
|
XP_006717693.1:p.Gly645AspfsTer2
|
|
XM_006717631.4:c.*56_*57insACTA
|
XP_006717694.1:n.*56_*57insACTA
|
|
XM_011539291.3:c.2629_2630insACTA
|
XP_011537593.1:p.Gly877AspfsTer2
|
|
XR_945604.3:n.2872_2873insACTA
|
|
|
XR_945605.3:n.2872_2873insACTA
|
|
|