ENST00000394867.9:n.1238A>T
|
|
|
ENST00000687128.1:n.1238A>T
|
|
|
ENST00000688002.1:n.1093A>T
|
|
|
ENST00000689792.1:n.703A>T
|
|
|
ENST00000262948.10:c.799A>T
MANE Select
|
ENSP00000262948.4:p.Ile267Phe
|
|
ENST00000262948.9:c.799A>T
|
ENSP00000262948.3:p.Ile267Phe
|
|
ENST00000394867.8:c.508A>T
|
ENSP00000378336.1:p.Ile170Phe
|
|
ENST00000593364.5:n.746A>T
|
|
|
ENST00000595715.1:n.614A>T
|
|
|
ENST00000597263.5:n.169+1698A>T
|
|
|
ENST00000599021.1:c.29+1698A>T
|
|
|
ENST00000600584.5:n.1359A>T
|
|
|
ENST00000601786.5:n.1100A>T
|
|
|
NM_030662.3:c.799A>T , LRG_750t1:c.799A>T
|
NP_109587.1:p.Ile267Phe
|
|
XM_006722799.2:c.705+1698A>T
|
XP_006722862.1:n.705+1698A>T
|
|
XM_011528133.1:c.229A>T
|
XP_011526435.1:p.Ile77Phe
|
|
XM_017026989.1:c.799A>T
|
XP_016882478.1:p.Ile267Phe
|
|
XM_017026990.1:c.705+1698A>T
|
XP_016882479.1:n.705+1698A>T
|
|
NM_030662.4:c.799A>T
MANE Select
|
NP_109587.1:p.Ile267Phe
|
|