ENST00000375708.4:c.2782_2783delinsGA
MANE Select
|
ENSP00000364860.3:p.Asp928=
|
|
ENST00000375708.3:c.2782_2783delinsGA
|
ENSP00000364860.3:p.Asp928=
|
|
ENST00000375715.5:c.1920+442_1920+443delinsGA
|
ENSP00000364867.1:n.1920+442_1920+443delinsGA
|
|
ENST00000550066.5:n.3250_3251delinsGA
|
|
|
NM_004560.3:c.2782_2783delinsGA
|
NP_004551.2:p.Asp928=
|
|
XM_005252008.3:c.2362_2363delinsGA
|
XP_005252065.1:p.Asp788=
|
|
XM_005252009.3:c.1579_1580delinsGA
|
XP_005252066.1:p.Asp527=
|
|
XM_006717121.2:c.2362_2363delinsGA
|
XP_006717184.1:p.Asp788=
|
|
XM_011518721.1:c.2362_2363delinsGA
|
XP_011517023.1:p.Asp788=
|
|
XM_005252008.4:c.2362_2363delinsGA
|
XP_005252065.1:p.Asp788=
|
|
XM_006717121.3:c.2362_2363delinsGA
|
XP_006717184.1:p.Asp788=
|
|
XM_017014762.1:c.2773_2774delinsGA
|
XP_016870251.1:p.Asp925=
|
|
XM_017014763.1:c.2362_2363delinsGA
|
XP_016870252.1:p.Asp788=
|
|
NM_004560.4:c.2782_2783delinsGA
MANE Select
|
NP_004551.2:p.Asp928=
|
|