ENST00000650793.2:n.575C>A
|
|
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ENST00000697612.1:n.1253C>A
|
|
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ENST00000374881.3:c.384C>A
|
ENSP00000364015.2:p.Ala128=
|
|
ENST00000374882.8:c.396C>A
MANE Select
|
ENSP00000364016.4:p.Ala132=
|
|
ENST00000650411.1:n.1717C>A
|
|
|
ENST00000650793.1:n.575C>A
|
|
|
ENST00000374881.2:c.384C>A
|
ENSP00000364015.2:p.Ala128=
|
|
ENST00000374882.7:c.396C>A
|
ENSP00000364016.3:p.Ala132=
|
|
ENST00000395339.7:c.324C>A
|
ENSP00000378748.3:p.Ala108=
|
|
ENST00000484003.1:n.780C>A
|
|
|
NM_004159.4:c.384C>A
|
NP_004150.1:p.Ala128=
|
|
NM_148919.3:c.396C>A
|
NP_683720.2:p.Ala132=
|
|
NM_148919.4:c.396C>A
MANE Select
|
NP_683720.2:p.Ala132=
|
|
NM_004159.5:c.384C>A
|
NP_004150.1:p.Ala128=
|
|