ENST00000682565.1:c.7633T=
|
ENSP00000507671.1:p.Phe2545=
|
|
ENST00000682801.1:c.7633T=
|
ENSP00000507862.1:p.Phe2545=
|
|
ENST00000682859.1:c.7633T=
|
ENSP00000508222.1:p.Phe2545=
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|
ENST00000683791.1:c.1025T=
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|
|
ENST00000684460.1:c.5085T=
|
|
|
ENST00000684548.1:c.7633T=
|
ENSP00000507421.1:p.Phe2545=
|
|
ENST00000684590.1:c.2080T=
|
ENSP00000507376.1:p.Phe694=
|
|
ENST00000684656.1:c.5085T=
|
|
|
ENST00000613296.6:c.8014T=
MANE Select
|
ENSP00000482968.1:p.Phe2672=
|
|
ENST00000651434.1:c.896-29802T=
|
|
|
ENST00000423048.5:c.2845T=
|
ENSP00000399833.1:p.Phe949=
|
|
ENST00000484298.5:c.7888T=
|
ENSP00000478155.1:p.Phe2630=
|
|
ENST00000613296.4:c.8014T=
|
ENSP00000482968.1:p.Phe2672=
|
|
ENST00000614410.4:c.8014T=
|
ENSP00000479094.1:p.Phe2672=
|
|
ENST00000620466.4:n.1817T=
|
|
|
NM_015120.4:c.8017T= , LRG_741t1:c.8017T=
|
NP_055935.4:p.Phe2673=
|
|
NM_001378454.1:c.8014T=
MANE Select
|
NP_001365383.1:p.Phe2672=
|
|