ENST00000682565.1:c.7655G=
|
ENSP00000507671.1:p.Trp2552=
|
|
ENST00000682801.1:c.7655G=
|
ENSP00000507862.1:p.Trp2552=
|
|
ENST00000682859.1:c.7655G=
|
ENSP00000508222.1:p.Trp2552=
|
|
ENST00000683791.1:c.1047G=
|
|
|
ENST00000684460.1:c.5107G=
|
|
|
ENST00000684548.1:c.7655G=
|
ENSP00000507421.1:p.Trp2552=
|
|
ENST00000684590.1:c.2102G=
|
ENSP00000507376.1:p.Trp701=
|
|
ENST00000684656.1:c.5107G=
|
|
|
ENST00000613296.6:c.8036G=
MANE Select
|
ENSP00000482968.1:p.Trp2679=
|
|
ENST00000651434.1:c.896-29780G=
|
|
|
ENST00000423048.5:c.2867G=
|
ENSP00000399833.1:p.Trp956=
|
|
ENST00000484298.5:c.7910G=
|
ENSP00000478155.1:p.Trp2637=
|
|
ENST00000613296.4:c.8036G=
|
ENSP00000482968.1:p.Trp2679=
|
|
ENST00000614410.4:c.8036G=
|
ENSP00000479094.1:p.Trp2679=
|
|
ENST00000620466.4:n.1839G=
|
|
|
NM_015120.4:c.8039G= , LRG_741t1:c.8039G=
|
NP_055935.4:p.Trp2680=
|
|
NM_001378454.1:c.8036G=
MANE Select
|
NP_001365383.1:p.Trp2679=
|
|