ENST00000683572.1:n.770G>T
|
|
|
ENST00000341947.7:c.4964G>T
MANE Select
|
ENSP00000339915.2:p.Cys1655Phe
|
|
ENST00000341947.6:c.4964G>T
|
ENSP00000339915.2:p.Cys1655Phe
|
|
ENST00000361917.5:c.4643G>T
|
ENSP00000355123.1:p.Cys1548Phe
|
|
ENST00000374708.8:c.4706G>T
|
ENSP00000363840.4:p.Cys1569Phe
|
|
ENST00000477772.1:n.754G>T
|
|
|
NM_080679.2:c.4643G>T
|
NP_542410.2:p.Cys1548Phe
|
|
NM_080680.2:c.4964G>T
|
NP_542411.2:p.Cys1655Phe
|
|
NM_080681.2:c.4706G>T
|
NP_542412.2:p.Cys1569Phe
|
|
XM_011514298.1:c.4118G>T
|
XP_011512600.1:p.Cys1373Phe
|
|
XM_011514299.1:c.4250G>T
|
XP_011512601.1:p.Cys1417Phe
|
|
XM_011514300.1:c.4070G>T
|
XP_011512602.1:p.Cys1357Phe
|
|
XM_011514301.1:c.4007G>T
|
XP_011512603.1:p.Cys1336Phe
|
|
XM_011514302.1:c.3851G>T
|
XP_011512604.1:p.Cys1284Phe
|
|
XM_011514299.2:c.4250G>T
|
XP_011512601.1:p.Cys1417Phe
|
|
XM_011514300.2:c.4070G>T
|
XP_011512602.1:p.Cys1357Phe
|
|
XM_011514302.2:c.3851G>T
|
XP_011512604.1:p.Cys1284Phe
|
|
XM_017010250.1:c.4964G>T
|
XP_016865739.1:p.Cys1655Phe
|
|
XM_017010251.2:c.3782G>T
|
XP_016865740.1:p.Cys1261Phe
|
|
NM_080680.3:c.4964G>T
MANE Select
|
NP_542411.2:p.Cys1655Phe
|
|
NM_080681.3:c.4706G>T
|
NP_542412.2:p.Cys1569Phe
|
|
NM_080679.3:c.4643G>T
|
NP_542410.2:p.Cys1548Phe
|
|