ENST00000394867.9:n.1579C>A
|
|
|
ENST00000688002.1:n.3291C>A
|
|
|
ENST00000688751.1:n.276C>A
|
|
|
ENST00000689792.1:n.1044C>A
|
|
|
ENST00000262948.10:c.1140C>A
MANE Select
|
ENSP00000262948.4:p.Ala380=
|
|
ENST00000262948.9:c.1140C>A
|
ENSP00000262948.3:p.Ala380=
|
|
ENST00000394867.8:c.849C>A
|
ENSP00000378336.1:p.Ala283=
|
|
ENST00000597263.5:n.325C>A
|
|
|
ENST00000599021.1:c.250C>A
|
|
|
ENST00000600584.5:n.2589C>A
|
|
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ENST00000601786.5:n.1441C>A
|
|
|
NM_030662.3:c.1140C>A , LRG_750t1:c.1140C>A
|
NP_109587.1:p.Ala380=
|
|
XM_006722799.2:c.861C>A
|
XP_006722862.1:p.Ala287=
|
|
XM_011528133.1:c.570C>A
|
XP_011526435.1:p.Ala190=
|
|
NM_030662.4:c.1140C>A
MANE Select
|
NP_109587.1:p.Ala380=
|
|