ENST00000682565.1:c.10606T=
|
ENSP00000507671.1:p.Trp3536=
|
|
ENST00000682801.1:c.10606T=
|
ENSP00000507862.1:p.Trp3536=
|
|
ENST00000682859.1:c.10606T=
|
ENSP00000508222.1:p.Trp3536=
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|
ENST00000683791.1:c.3692T=
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|
|
ENST00000684460.1:c.7887T=
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|
|
ENST00000684548.1:c.10606T=
|
ENSP00000507421.1:p.Trp3536=
|
|
ENST00000684590.1:c.5053T=
|
ENSP00000507376.1:p.Trp1685=
|
|
ENST00000684656.1:c.7932T=
|
|
|
ENST00000613296.6:c.10987T=
MANE Select
|
ENSP00000482968.1:p.Trp3663=
|
|
ENST00000651057.1:c.1141T=
|
ENSP00000498504.1:p.Trp381=
|
|
ENST00000651434.1:c.2343T=
|
|
|
ENST00000651750.1:c.375T=
|
|
|
ENST00000652487.1:c.2084T=
|
|
|
ENST00000423048.5:c.4478T=
|
ENSP00000399833.1:n.4478T=
|
|
ENST00000484298.5:c.10861T=
|
ENSP00000478155.1:p.Trp3621=
|
|
ENST00000613296.4:c.10987T=
|
ENSP00000482968.1:p.Trp3663=
|
|
ENST00000614410.4:c.10987T=
|
ENSP00000479094.1:p.Trp3663=
|
|
ENST00000620466.4:n.4790T=
|
|
|
NM_015120.4:c.10990T= , LRG_741t1:c.10990T=
|
NP_055935.4:p.Trp3664=
|
|
NM_001378454.1:c.10987T=
MANE Select
|
NP_001365383.1:p.Trp3663=
|
|