ENST00000642683.1:c.734T=
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ENSP00000495376.1:p.Leu245=
|
|
ENST00000643672.1:c.731T=
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ENSP00000494532.1:p.Leu244=
|
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ENST00000645280.1:c.728T=
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ENSP00000496690.1:p.Leu243=
|
|
ENST00000648579.1:c.*79T=
|
ENSP00000497638.1:n.*79T=
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|
ENST00000650617.1:c.782T=
MANE Select
|
ENSP00000497532.1:p.Leu261=
|
|
ENST00000273158.8:c.782T=
|
ENSP00000273158.3:p.Leu261=
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|
NM_017875.2:c.782T=
|
NP_060345.2:p.Leu261=
|
|
XM_006713214.1:c.770T=
|
XP_006713277.1:p.Leu257=
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|
XM_011533869.1:c.764T=
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XP_011532171.1:p.Leu255=
|
|
XM_011533870.1:c.731T=
|
XP_011532172.1:p.Leu244=
|
|
XM_011533871.1:c.602T=
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XP_011532173.1:p.Leu201=
|
|
NM_001354798.1:c.626-1832T=
|
NP_001341727.1:n.626-1832T=
|
|
NM_017875.4:c.782T=
MANE Select
|
NP_060345.2:p.Leu261=
|
|
XM_006713214.2:c.770T=
|
XP_006713277.1:p.Leu257=
|
|
XM_011533869.2:c.764T=
|
XP_011532171.1:p.Leu255=
|
|
XM_024453611.1:c.728T=
|
XP_024309379.1:p.Leu243=
|
|
NM_001354798.2:c.626-1832T=
|
NP_001341727.1:n.626-1832T=
|
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