ENST00000682565.1:c.10170T=
|
ENSP00000507671.1:p.His3390=
|
|
ENST00000682801.1:c.10170T=
|
ENSP00000507862.1:p.His3390=
|
|
ENST00000682859.1:c.10170T=
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ENSP00000508222.1:p.His3390=
|
|
ENST00000683791.1:c.3256T=
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|
|
ENST00000684460.1:c.7451T=
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|
|
ENST00000684548.1:c.10170T=
|
ENSP00000507421.1:p.His3390=
|
|
ENST00000684590.1:c.4617T=
|
ENSP00000507376.1:p.His1539=
|
|
ENST00000684656.1:c.7496T=
|
|
|
ENST00000613296.6:c.10551T=
MANE Select
|
ENSP00000482968.1:p.His3517=
|
|
ENST00000651057.1:c.705T=
|
ENSP00000498504.1:p.His235=
|
|
ENST00000651434.1:c.1907T=
|
|
|
ENST00000652487.1:c.1648T=
|
|
|
ENST00000423048.5:c.4042T=
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ENSP00000399833.1:n.4042T=
|
|
ENST00000484298.5:c.10425T=
|
ENSP00000478155.1:p.His3475=
|
|
ENST00000613296.4:c.10551T=
|
ENSP00000482968.1:p.His3517=
|
|
ENST00000614410.4:c.10551T=
|
ENSP00000479094.1:p.His3517=
|
|
ENST00000620466.4:n.4354T=
|
|
|
NM_015120.4:c.10554T= , LRG_741t1:c.10554T=
|
NP_055935.4:p.His3518=
|
|
NM_001378454.1:c.10551T=
MANE Select
|
NP_001365383.1:p.His3517=
|
|