ENST00000394867.9:n.1181T>A
|
|
|
ENST00000687128.1:n.1181T>A
|
|
|
ENST00000688002.1:n.1036T>A
|
|
|
ENST00000689792.1:n.646T>A
|
|
|
ENST00000262948.10:c.742T>A
MANE Select
|
ENSP00000262948.4:p.Ser248Thr
|
|
ENST00000262948.9:c.742T>A
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ENSP00000262948.3:p.Ser248Thr
|
|
ENST00000394867.8:c.451T>A
|
ENSP00000378336.1:p.Ser151Thr
|
|
ENST00000593364.5:n.689T>A
|
|
|
ENST00000595715.1:n.557T>A
|
|
|
ENST00000597263.5:n.169+1641T>A
|
|
|
ENST00000599021.1:c.29+1641T>A
|
|
|
ENST00000600584.5:n.1302T>A
|
|
|
ENST00000601786.5:n.1043T>A
|
|
|
NM_030662.3:c.742T>A , LRG_750t1:c.742T>A
|
NP_109587.1:p.Ser248Thr
|
|
XM_006722799.2:c.705+1641T>A
|
XP_006722862.1:n.705+1641T>A
|
|
XM_011528133.1:c.172T>A
|
XP_011526435.1:p.Ser58Thr
|
|
XM_017026989.1:c.742T>A
|
XP_016882478.1:p.Ser248Thr
|
|
XM_017026990.1:c.705+1641T>A
|
XP_016882479.1:n.705+1641T>A
|
|
NM_030662.4:c.742T>A
MANE Select
|
NP_109587.1:p.Ser248Thr
|
|