ENST00000272602.7:c.513G>A
MANE Select
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ENSP00000272602.2:p.Trp171Ter
|
|
ENST00000272602.6:c.513G>A
|
ENSP00000272602.2:p.Trp171Ter
|
|
ENST00000393503.2:n.518G>A
|
|
|
ENST00000393504.5:c.513G>A
|
ENSP00000377140.1:p.Trp171Ter
|
|
ENST00000409937.1:c.525G>A
|
ENSP00000386761.1:p.Trp175Ter
|
|
ENST00000436404.6:c.459G>A
|
ENSP00000410070.2:p.Trp153Ter
|
|
NM_001079878.1:c.459G>A
|
NP_001073347.1:p.Trp153Ter
|
|
NM_001298.2:c.513G>A
|
NP_001289.1:p.Trp171Ter
|
|
XM_006712243.2:c.624G>A
|
XP_006712306.1:p.Trp208Ter
|
|
XM_011510554.1:c.678G>A
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XP_011508856.1:p.Trp226Ter
|
|
XM_011510554.2:c.678G>A
|
XP_011508856.1:p.Trp226Ter
|
|
NM_001079878.2:c.459G>A
|
NP_001073347.1:p.Trp153Ter
|
|
NM_001298.3:c.513G>A
MANE Select
|
NP_001289.1:p.Trp171Ter
|
|