ENST00000375708.4:c.2748_2750dup
MANE Select
|
ENSP00000364860.3:p.Glu917_Gly918insGlu
|
|
ENST00000375708.3:c.2748_2750dup
|
ENSP00000364860.3:p.Glu917_Gly918insGlu
|
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ENST00000375715.5:c.1920+408_1920+410dup
|
ENSP00000364867.1:n.1920+408_1920+410dup
|
|
ENST00000550066.5:n.3216_3218dup
|
|
|
NM_004560.3:c.2748_2750dup
|
NP_004551.2:p.Glu917_Gly918insGlu
|
|
XM_005252008.3:c.2328_2330dup
|
XP_005252065.1:p.Glu777_Gly778insGlu
|
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XM_005252009.3:c.1545_1547dup
|
XP_005252066.1:p.Glu516_Gly517insGlu
|
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XM_006717121.2:c.2328_2330dup
|
XP_006717184.1:p.Glu777_Gly778insGlu
|
|
XM_011518721.1:c.2328_2330dup
|
XP_011517023.1:p.Glu777_Gly778insGlu
|
|
XM_005252008.4:c.2328_2330dup
|
XP_005252065.1:p.Glu777_Gly778insGlu
|
|
XM_006717121.3:c.2328_2330dup
|
XP_006717184.1:p.Glu777_Gly778insGlu
|
|
XM_017014762.1:c.2739_2741dup
|
XP_016870251.1:p.Glu914_Gly915insGlu
|
|
XM_017014763.1:c.2328_2330dup
|
XP_016870252.1:p.Glu777_Gly778insGlu
|
|
NM_004560.4:c.2748_2750dup
MANE Select
|
NP_004551.2:p.Glu917_Gly918insGlu
|
|