ENST00000225964.10:c.1703_1704delinsCA
MANE Select
|
ENSP00000225964.6:p.Pro568=
|
|
ENST00000225964.9:c.1703_1704delinsCA
|
ENSP00000225964.5:p.Pro568=
|
|
ENST00000463440.1:n.93_94delinsCA
|
|
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ENST00000471344.1:n.735_736delinsCA
|
|
|
ENST00000476387.1:n.52_53delinsCA
|
|
|
NM_000088.3:c.1703_1704delinsCA , LRG_1t1:c.1703_1704delinsCA
|
NP_000079.2:p.Pro568=
|
|
XM_005257058.3:c.1703_1704delinsCA
|
XP_005257115.2:p.Pro568=
|
|
XM_005257059.3:c.958-1314_958-1313delinsCA
|
XP_005257116.2:n.958-1314_958-1313delinsCA
|
|
XM_011524341.1:c.1505_1506delinsCA
|
XP_011522643.1:p.Pro502=
|
|
XM_005257058.4:c.1703_1704delinsCA
|
XP_005257115.2:p.Pro568=
|
|
XM_005257059.4:c.958-1314_958-1313delinsCA
|
XP_005257116.2:n.958-1314_958-1313delinsCA
|
|
NM_000088.4:c.1703_1704delinsCA
MANE Select
|
NP_000079.2:p.Pro568=
|
|