ENST00000255078.8:c.368A>T
MANE Select
|
ENSP00000255078.4:p.Asp123Val
|
|
ENST00000539224.2:c.331A>T
|
|
|
ENST00000674583.1:c.331A>T
|
|
|
ENST00000674597.1:c.179A>T
|
|
|
ENST00000674955.1:c.368A>T
|
ENSP00000502463.1:p.Asp123Val
|
|
ENST00000675142.1:n.331A>T
|
|
|
ENST00000675469.1:c.244A>T
|
|
|
ENST00000675615.1:c.368A>T
|
ENSP00000502413.1:p.Asp123Val
|
|
ENST00000675674.1:n.331A>T
|
|
|
ENST00000675873.1:c.331A>T
|
|
|
ENST00000676173.1:n.412A>T
|
|
|
ENST00000676228.1:c.368A>T
|
ENSP00000502375.1:p.Asp123Val
|
|
ENST00000255078.7:c.368A>T
|
ENSP00000255078.3:p.Asp123Val
|
|
ENST00000539224.1:c.368A>T
|
ENSP00000440465.1:p.Asp123Val
|
|
ENST00000544541.1:c.*108A>T
|
ENSP00000443343.1:n.*108A>T
|
|
NM_002180.2:c.368A>T , LRG_250t1:c.368A>T
|
NP_002171.2:p.Asp123Val
|
|
XM_005273974.2:c.-644A>T
|
XP_005274031.1:n.-644A>T
|
|
XM_005273976.1:c.368A>T
|
XP_005274033.1:p.Asp123Val
|
|
XR_247198.1:n.470A>T
|
|
|
XR_949903.1:n.470A>T
|
|
|
XM_005273976.2:c.368A>T
|
XP_005274033.1:p.Asp123Val
|
|
XM_017017669.2:c.-546A>T
|
XP_016873158.1:n.-546A>T
|
|
XM_017017671.2:c.368A>T
|
XP_016873160.1:p.Asp123Val
|
|
XR_949903.3:n.466A>T
|
|
|
NM_002180.3:c.368A>T
MANE Select
|
NP_002171.2:p.Asp123Val
|
|