ENST00000683572.1:n.683A>T
|
|
|
ENST00000341947.7:c.4877A>T
MANE Select
|
ENSP00000339915.2:p.Asp1626Val
|
|
ENST00000341947.6:c.4877A>T
|
ENSP00000339915.2:p.Asp1626Val
|
|
ENST00000361917.5:c.4556A>T
|
ENSP00000355123.1:p.Asp1519Val
|
|
ENST00000374708.8:c.4619A>T
|
ENSP00000363840.4:p.Asp1540Val
|
|
ENST00000477772.1:n.667A>T
|
|
|
NM_080679.2:c.4556A>T
|
NP_542410.2:p.Asp1519Val
|
|
NM_080680.2:c.4877A>T
|
NP_542411.2:p.Asp1626Val
|
|
NM_080681.2:c.4619A>T
|
NP_542412.2:p.Asp1540Val
|
|
XM_011514298.1:c.4031A>T
|
XP_011512600.1:p.Asp1344Val
|
|
XM_011514299.1:c.4163A>T
|
XP_011512601.1:p.Asp1388Val
|
|
XM_011514300.1:c.3983A>T
|
XP_011512602.1:p.Asp1328Val
|
|
XM_011514301.1:c.3920A>T
|
XP_011512603.1:p.Asp1307Val
|
|
XM_011514302.1:c.3764A>T
|
XP_011512604.1:p.Asp1255Val
|
|
XM_011514299.2:c.4163A>T
|
XP_011512601.1:p.Asp1388Val
|
|
XM_011514300.2:c.3983A>T
|
XP_011512602.1:p.Asp1328Val
|
|
XM_011514302.2:c.3764A>T
|
XP_011512604.1:p.Asp1255Val
|
|
XM_017010250.1:c.4877A>T
|
XP_016865739.1:p.Asp1626Val
|
|
XM_017010251.2:c.3695A>T
|
XP_016865740.1:p.Asp1232Val
|
|
NM_080680.3:c.4877A>T
MANE Select
|
NP_542411.2:p.Asp1626Val
|
|
NM_080681.3:c.4619A>T
|
NP_542412.2:p.Asp1540Val
|
|
NM_080679.3:c.4556A>T
|
NP_542410.2:p.Asp1519Val
|
|