ENST00000394867.9:n.1560T>G
|
|
|
ENST00000688002.1:n.3272T>G
|
|
|
ENST00000688751.1:n.257T>G
|
|
|
ENST00000689792.1:n.1025T>G
|
|
|
ENST00000262948.10:c.1121T>G
MANE Select
|
ENSP00000262948.4:p.Val374Gly
|
|
ENST00000262948.9:c.1121T>G
|
ENSP00000262948.3:p.Val374Gly
|
|
ENST00000394867.8:c.830T>G
|
ENSP00000378336.1:p.Val277Gly
|
|
ENST00000597263.5:n.306T>G
|
|
|
ENST00000599021.1:c.231T>G
|
|
|
ENST00000600584.5:n.2570T>G
|
|
|
ENST00000601786.5:n.1422T>G
|
|
|
NM_030662.3:c.1121T>G , LRG_750t1:c.1121T>G
|
NP_109587.1:p.Val374Gly
|
|
XM_006722799.2:c.842T>G
|
XP_006722862.1:p.Val281Gly
|
|
XM_011528133.1:c.551T>G
|
XP_011526435.1:p.Val184Gly
|
|
NM_030662.4:c.1121T>G
MANE Select
|
NP_109587.1:p.Val374Gly
|
|