ENST00000683572.1:n.656A>T
|
|
|
ENST00000341947.7:c.4850A>T
MANE Select
|
ENSP00000339915.2:p.Asp1617Val
|
|
ENST00000341947.6:c.4850A>T
|
ENSP00000339915.2:p.Asp1617Val
|
|
ENST00000361917.5:c.4529A>T
|
ENSP00000355123.1:p.Asp1510Val
|
|
ENST00000374708.8:c.4592A>T
|
ENSP00000363840.4:p.Asp1531Val
|
|
ENST00000477772.1:n.640A>T
|
|
|
NM_080679.2:c.4529A>T
|
NP_542410.2:p.Asp1510Val
|
|
NM_080680.2:c.4850A>T
|
NP_542411.2:p.Asp1617Val
|
|
NM_080681.2:c.4592A>T
|
NP_542412.2:p.Asp1531Val
|
|
XM_011514298.1:c.4004A>T
|
XP_011512600.1:p.Asp1335Val
|
|
XM_011514299.1:c.4136A>T
|
XP_011512601.1:p.Asp1379Val
|
|
XM_011514300.1:c.3956A>T
|
XP_011512602.1:p.Asp1319Val
|
|
XM_011514301.1:c.3893A>T
|
XP_011512603.1:p.Asp1298Val
|
|
XM_011514302.1:c.3737A>T
|
XP_011512604.1:p.Asp1246Val
|
|
XM_011514299.2:c.4136A>T
|
XP_011512601.1:p.Asp1379Val
|
|
XM_011514300.2:c.3956A>T
|
XP_011512602.1:p.Asp1319Val
|
|
XM_011514302.2:c.3737A>T
|
XP_011512604.1:p.Asp1246Val
|
|
XM_017010250.1:c.4850A>T
|
XP_016865739.1:p.Asp1617Val
|
|
XM_017010251.2:c.3668A>T
|
XP_016865740.1:p.Asp1223Val
|
|
NM_080680.3:c.4850A>T
MANE Select
|
NP_542411.2:p.Asp1617Val
|
|
NM_080681.3:c.4592A>T
|
NP_542412.2:p.Asp1531Val
|
|
NM_080679.3:c.4529A>T
|
NP_542410.2:p.Asp1510Val
|
|