ENST00000426263.10:c.477G=
MANE Select
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ENSP00000416293.2:p.Leu159=
|
|
ENST00000674765.1:c.477G=
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ENSP00000501811.1:p.Leu159=
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|
ENST00000675112.1:n.500G=
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|
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ENST00000676254.1:n.926G=
|
|
|
ENST00000426263.7:c.477G=
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ENSP00000416293.2:p.Leu159=
|
|
ENST00000439722.2:c.356G=
|
ENSP00000395521.2:n.356G=
|
|
ENST00000475162.3:c.376G=
|
|
|
ENST00000625233.2:n.685G=
|
|
|
ENST00000630287.2:c.477G=
|
ENSP00000486694.1:p.Leu159=
|
|
NM_006516.2:c.477G=
|
NP_006507.2:p.Leu159=
|
|
NM_006516.3:c.477G=
|
NP_006507.2:p.Leu159=
|
|
NM_006516.4:c.477G=
MANE Select
|
NP_006507.2:p.Leu159=
|
|