ENST00000682565.1:c.7969G>T
|
ENSP00000507671.1:p.Glu2657Ter
|
|
ENST00000682801.1:c.7969G>T
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ENSP00000507862.1:p.Glu2657Ter
|
|
ENST00000682859.1:c.7969G>T
|
ENSP00000508222.1:p.Glu2657Ter
|
|
ENST00000683791.1:c.1361G>T
|
|
|
ENST00000684460.1:c.5421G>T
|
|
|
ENST00000684548.1:c.7969G>T
|
ENSP00000507421.1:p.Glu2657Ter
|
|
ENST00000684590.1:c.2416G>T
|
ENSP00000507376.1:p.Glu806Ter
|
|
ENST00000684656.1:c.5421G>T
|
|
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ENST00000613296.6:c.8350G>T
MANE Select
|
ENSP00000482968.1:p.Glu2784Ter
|
|
ENST00000651434.1:c.896-29466G>T
|
|
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ENST00000423048.5:c.3030+151G>T
|
ENSP00000399833.1:n.3030+151G>T
|
|
ENST00000484298.5:c.8224G>T
|
ENSP00000478155.1:p.Glu2742Ter
|
|
ENST00000613296.4:c.8350G>T
|
ENSP00000482968.1:p.Glu2784Ter
|
|
ENST00000614410.4:c.8350G>T
|
ENSP00000479094.1:p.Glu2784Ter
|
|
ENST00000620466.4:n.2153G>T
|
|
|
NM_015120.4:c.8353G>T , LRG_741t1:c.8353G>T
|
NP_055935.4:p.Glu2785Ter
|
|
NM_001378454.1:c.8350G>T
MANE Select
|
NP_001365383.1:p.Glu2784Ter
|
|