ENST00000682565.1:c.10551C=
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ENSP00000507671.1:p.Leu3517=
|
|
ENST00000682801.1:c.10551C=
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ENSP00000507862.1:p.Leu3517=
|
|
ENST00000682859.1:c.10551C=
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ENSP00000508222.1:p.Leu3517=
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ENST00000683791.1:c.3637C=
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|
|
ENST00000684460.1:c.7832C=
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|
|
ENST00000684548.1:c.10551C=
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ENSP00000507421.1:p.Leu3517=
|
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ENST00000684590.1:c.4998C=
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ENSP00000507376.1:p.Leu1666=
|
|
ENST00000684656.1:c.7877C=
|
|
|
ENST00000613296.6:c.10932C=
MANE Select
|
ENSP00000482968.1:p.Leu3644=
|
|
ENST00000651057.1:c.1086C=
|
ENSP00000498504.1:p.Leu362=
|
|
ENST00000651434.1:c.2288C=
|
|
|
ENST00000651750.1:c.320C=
|
|
|
ENST00000652487.1:c.2029C=
|
|
|
ENST00000423048.5:c.4423C=
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ENSP00000399833.1:n.4423C=
|
|
ENST00000484298.5:c.10806C=
|
ENSP00000478155.1:p.Leu3602=
|
|
ENST00000613296.4:c.10932C=
|
ENSP00000482968.1:p.Leu3644=
|
|
ENST00000614410.4:c.10932C=
|
ENSP00000479094.1:p.Leu3644=
|
|
ENST00000620466.4:n.4735C=
|
|
|
NM_015120.4:c.10935C= , LRG_741t1:c.10935C=
|
NP_055935.4:p.Leu3645=
|
|
NM_001378454.1:c.10932C=
MANE Select
|
NP_001365383.1:p.Leu3644=
|
|