ENST00000375708.4:c.2748_2751delinsGGAA
MANE Select
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ENSP00000364860.3:p.Glu916=
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|
ENST00000375708.3:c.2748_2751delinsGGAA
|
ENSP00000364860.3:p.Glu916=
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|
ENST00000375715.5:c.1920+408_1920+411delinsGGAA
|
ENSP00000364867.1:n.1920+408_1920+411delinsGGAA
|
|
ENST00000550066.5:n.3216_3219delinsGGAA
|
|
|
NM_004560.3:c.2748_2751delinsGGAA
|
NP_004551.2:p.Glu916=
|
|
XM_005252008.3:c.2328_2331delinsGGAA
|
XP_005252065.1:p.Glu776=
|
|
XM_005252009.3:c.1545_1548delinsGGAA
|
XP_005252066.1:p.Glu515=
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|
XM_006717121.2:c.2328_2331delinsGGAA
|
XP_006717184.1:p.Glu776=
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|
XM_011518721.1:c.2328_2331delinsGGAA
|
XP_011517023.1:p.Glu776=
|
|
XM_005252008.4:c.2328_2331delinsGGAA
|
XP_005252065.1:p.Glu776=
|
|
XM_006717121.3:c.2328_2331delinsGGAA
|
XP_006717184.1:p.Glu776=
|
|
XM_017014762.1:c.2739_2742delinsGGAA
|
XP_016870251.1:p.Glu913=
|
|
XM_017014763.1:c.2328_2331delinsGGAA
|
XP_016870252.1:p.Glu776=
|
|
NM_004560.4:c.2748_2751delinsGGAA
MANE Select
|
NP_004551.2:p.Glu916=
|
|