ENST00000561514.3:c.1692_1693delinsGA
|
ENSP00000460666.3:p.Gly564=
|
|
ENST00000565038.2:c.212-1193_212-1192delinsGA
|
ENSP00000459882.2:n.212-1193_212-1192delinsGA
|
|
ENST00000566069.6:c.1686_1687delinsGA
|
ENSP00000459237.2:p.Gly562=
|
|
ENST00000697377.2:c.1692_1693delinsGA
|
ENSP00000513286.2:p.Gly564=
|
|
ENST00000697379.2:c.1692_1693delinsGA
|
ENSP00000513287.2:p.Gly564=
|
|
ENST00000561514.2:c.801_802delinsGA
|
ENSP00000460666.2:p.Gly267=
|
|
ENST00000697374.1:c.801_802delinsGA
|
ENSP00000513284.1:p.Gly267=
|
|
ENST00000697375.1:n.3033_3034delinsGA
|
|
|
ENST00000697376.1:c.801_802delinsGA
|
ENSP00000513285.1:p.Gly267=
|
|
ENST00000697377.1:c.801_802delinsGA
|
ENSP00000513286.1:p.Gly267=
|
|
ENST00000697378.1:n.2206_2207delinsGA
|
|
|
ENST00000697379.1:c.801_802delinsGA
|
ENSP00000513287.1:p.Gly267=
|
|
ENST00000697380.1:n.614_615delinsGA
|
|
|
ENST00000697381.1:n.381_382delinsGA
|
|
|
ENST00000697382.1:c.801_802delinsGA
|
ENSP00000513288.1:p.Gly267=
|
|
ENST00000697383.1:c.49-1193_49-1192delinsGA
|
ENSP00000513289.1:n.49-1193_49-1192delinsGA
|
|
ENST00000697384.1:n.1840_1841delinsGA
|
|
|
ENST00000261584.9:c.1686_1687delinsGA
MANE Select
|
ENSP00000261584.4:p.Gly562=
|
|
ENST00000261584.8:c.1686_1687delinsGA
|
ENSP00000261584.4:p.Gly562=
|
|
ENST00000565038.1:c.87-1193_87-1192delinsGA
|
|
|
ENST00000568219.5:c.801_802delinsGA
|
ENSP00000454703.2:p.Gly267=
|
|
NM_024675.3:c.1686_1687delinsGA , LRG_308t1:c.1686_1687delinsGA
|
NP_078951.2:p.Gly562=
|
|
XM_011545946.1:c.1692_1693delinsGA
|
XP_011544248.1:p.Gly564=
|
|
XM_011545947.1:c.1692_1693delinsGA
|
XP_011544249.1:p.Gly564=
|
|
XM_011545948.1:c.801_802delinsGA
|
XP_011544250.1:p.Gly267=
|
|
XR_950851.1:n.2482_2483delinsGA
|
|
|
XM_011545946.2:c.1692_1693delinsGA
|
XP_011544248.1:p.Gly564=
|
|
XM_011545947.2:c.1692_1693delinsGA
|
XP_011544249.1:p.Gly564=
|
|
XM_011545948.2:c.801_802delinsGA
|
XP_011544250.1:p.Gly267=
|
|
XM_017023671.1:c.1692_1693delinsGA
|
XP_016879160.1:p.Gly564=
|
|
XM_017023672.2:c.1686_1687delinsGA
|
XP_016879161.1:p.Gly562=
|
|
XM_017023673.2:c.1686_1687delinsGA
|
XP_016879162.1:p.Gly562=
|
|
NM_024675.4:c.1686_1687delinsGA
MANE Select
|
NP_078951.2:p.Gly562=
|
|