ENST00000389857.11:c.3288dup
MANE Select
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ENSP00000374507.6:p.Leu1097ThrfsTer?
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ENST00000389857.10:c.3288dup
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ENSP00000374507.6:p.Leu1097ThrfsTer?
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NM_001080414.3:c.3288dup
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NP_001073883.2:p.Leu1097ThrfsTer?
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|
XM_005267691.3:c.3288dup
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XP_005267748.1:p.Leu1097ThrfsTer?
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XM_011536796.1:c.3180dup
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XP_011535098.1:p.Leu1061ThrfsTer?
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XR_429316.2:n.3416dup
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|
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XR_943459.1:n.3416dup
|
|
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XM_005267691.5:c.3288dup
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XP_005267748.1:p.Leu1097ThrfsTer?
|
|
XM_011536796.2:c.3180dup
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XP_011535098.1:p.Leu1061ThrfsTer?
|
|
XM_017021335.2:c.3288dup
|
XP_016876824.1:p.Leu1097ThrfsTer?
|
|
XM_017021336.1:c.369dup
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XP_016876825.1:p.Leu124ThrfsTer?
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XR_429316.4:n.3414dup
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|
|
NM_001080414.4:c.3288dup
MANE Select
|
NP_001073883.2:p.Leu1097ThrfsTer?
|
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