ENST00000426263.10:c.372G>A
MANE Select
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ENSP00000416293.2:p.Leu124=
|
|
ENST00000674765.1:c.372G>A
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ENSP00000501811.1:p.Leu124=
|
|
ENST00000675112.1:n.395G>A
|
|
|
ENST00000676254.1:n.821G>A
|
|
|
ENST00000372500.4:c.276G>A
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ENSP00000361578.4:p.Leu92=
|
|
ENST00000426263.7:c.372G>A
|
ENSP00000416293.2:p.Leu124=
|
|
ENST00000439722.2:c.251G>A
|
ENSP00000395521.2:n.251G>A
|
|
ENST00000475162.3:c.271G>A
|
|
|
ENST00000625233.2:n.580G>A
|
|
|
ENST00000630287.2:c.372G>A
|
ENSP00000486694.1:p.Leu124=
|
|
NM_006516.2:c.372G>A
|
NP_006507.2:p.Leu124=
|
|
NM_006516.3:c.372G>A
|
NP_006507.2:p.Leu124=
|
|
NM_006516.4:c.372G>A
MANE Select
|
NP_006507.2:p.Leu124=
|
|