ENST00000682565.1:c.10492T=
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ENSP00000507671.1:p.Leu3498=
|
|
ENST00000682801.1:c.10492T=
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ENSP00000507862.1:p.Leu3498=
|
|
ENST00000682859.1:c.10492T=
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ENSP00000508222.1:p.Leu3498=
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ENST00000683791.1:c.3578T=
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|
|
ENST00000684460.1:c.7773T=
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|
|
ENST00000684548.1:c.10492T=
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ENSP00000507421.1:p.Leu3498=
|
|
ENST00000684590.1:c.4939T=
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ENSP00000507376.1:p.Leu1647=
|
|
ENST00000684656.1:c.7818T=
|
|
|
ENST00000613296.6:c.10873T=
MANE Select
|
ENSP00000482968.1:p.Leu3625=
|
|
ENST00000651057.1:c.1027T=
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ENSP00000498504.1:p.Leu343=
|
|
ENST00000651434.1:c.2229T=
|
|
|
ENST00000651750.1:c.261T=
|
|
|
ENST00000652487.1:c.1970T=
|
|
|
ENST00000423048.5:c.4364T=
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ENSP00000399833.1:n.4364T=
|
|
ENST00000484298.5:c.10747T=
|
ENSP00000478155.1:p.Leu3583=
|
|
ENST00000613296.4:c.10873T=
|
ENSP00000482968.1:p.Leu3625=
|
|
ENST00000614410.4:c.10873T=
|
ENSP00000479094.1:p.Leu3625=
|
|
ENST00000620466.4:n.4676T=
|
|
|
NM_015120.4:c.10876T= , LRG_741t1:c.10876T=
|
NP_055935.4:p.Leu3626=
|
|
NM_001378454.1:c.10873T=
MANE Select
|
NP_001365383.1:p.Leu3625=
|
|