ENST00000378802.5:c.683_686delinsAGAT
MANE Select
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ENSP00000368079.4:p.Glu228=
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ENST00000378802.4:c.683_686delinsAGAT
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ENSP00000368079.4:p.Glu228=
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|
ENST00000507209.5:n.1524_1527delinsAGAT
|
|
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NM_207352.3:c.683_686delinsAGAT
|
NP_997235.3:p.Glu228=
|
|
XM_005262935.2:c.683_686delinsAGAT
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XP_005262992.1:p.Glu228=
|
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XM_006714184.2:c.287_290delinsAGAT
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XP_006714247.1:p.Glu96=
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XM_005262935.4:c.683_686delinsAGAT
|
XP_005262992.1:p.Glu228=
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XM_017008037.1:c.287_290delinsAGAT
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XP_016863526.1:p.Glu96=
|
|
NM_207352.4:c.683_686delinsAGAT
MANE Select
|
NP_997235.3:p.Glu228=
|
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