ENST00000433363.7:c.502G>T
MANE Select
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ENSP00000406220.2:p.Ala168Ser
|
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ENST00000293800.10:c.451G>T
|
ENSP00000293800.6:p.Ala151Ser
|
|
ENST00000381074.8:c.373G>T
|
ENSP00000370464.4:p.Ala125Ser
|
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ENST00000433363.6:c.502G>T
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ENSP00000406220.2:p.Ala168Ser
|
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ENST00000572094.1:c.*252G>T
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ENSP00000461495.1:n.*252G>T
|
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ENST00000572352.5:c.391G>T
|
ENSP00000461622.1:p.Ala131Ser
|
|
ENST00000573648.5:c.502G>T
|
ENSP00000459372.1:p.Ala168Ser
|
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ENST00000574824.5:n.1635G>T
|
|
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ENST00000576323.1:n.532G>T
|
|
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NM_001143838.2:c.502G>T
|
NP_001137310.1:p.Ala168Ser
|
|
NM_001284509.1:c.451G>T
|
NP_001271438.1:p.Ala151Ser
|
|
NM_001284510.1:c.373G>T
|
NP_001271439.1:p.Ala125Ser
|
|
NM_177550.4:c.502G>T , LRG_1020t1:c.502G>T
|
NP_808218.1:p.Ala168Ser
|
|
XM_006721504.2:c.391G>T
|
XP_006721567.1:p.Ala131Ser
|
|
XM_011523795.1:c.502G>T
|
XP_011522097.1:p.Ala168Ser
|
|
XM_011523795.3:c.502G>T
|
XP_011522097.1:p.Ala168Ser
|
|
NM_001143838.3:c.502G>T
|
NP_001137310.1:p.Ala168Ser
|
|
NM_001284509.2:c.451G>T
|
NP_001271438.1:p.Ala151Ser
|
|
NM_001284510.2:c.373G>T
|
NP_001271439.1:p.Ala125Ser
|
|
NM_177550.5:c.502G>T
MANE Select
|
NP_808218.1:p.Ala168Ser
|
|