ENST00000426263.10:c.366G>A
MANE Select
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ENSP00000416293.2:p.Leu122=
|
|
ENST00000674765.1:c.366G>A
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ENSP00000501811.1:p.Leu122=
|
|
ENST00000675112.1:n.389G>A
|
|
|
ENST00000676254.1:n.815G>A
|
|
|
ENST00000372500.4:c.270G>A
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ENSP00000361578.4:p.Leu90=
|
|
ENST00000426263.7:c.366G>A
|
ENSP00000416293.2:p.Leu122=
|
|
ENST00000439722.2:c.245G>A
|
ENSP00000395521.2:n.245G>A
|
|
ENST00000475162.3:c.265G>A
|
|
|
ENST00000625233.2:n.574G>A
|
|
|
ENST00000630287.2:c.366G>A
|
ENSP00000486694.1:p.Leu122=
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|
NM_006516.2:c.366G>A
|
NP_006507.2:p.Leu122=
|
|
NM_006516.3:c.366G>A
|
NP_006507.2:p.Leu122=
|
|
NM_006516.4:c.366G>A
MANE Select
|
NP_006507.2:p.Leu122=
|
|