ENST00000683572.1:n.614G>T
|
|
|
ENST00000341947.7:c.4808G>T
MANE Select
|
ENSP00000339915.2:p.Cys1603Phe
|
|
ENST00000341947.6:c.4808G>T
|
ENSP00000339915.2:p.Cys1603Phe
|
|
ENST00000361917.5:c.4487G>T
|
ENSP00000355123.1:p.Cys1496Phe
|
|
ENST00000374708.8:c.4550G>T
|
ENSP00000363840.4:p.Cys1517Phe
|
|
ENST00000477772.1:n.598G>T
|
|
|
NM_080679.2:c.4487G>T
|
NP_542410.2:p.Cys1496Phe
|
|
NM_080680.2:c.4808G>T
|
NP_542411.2:p.Cys1603Phe
|
|
NM_080681.2:c.4550G>T
|
NP_542412.2:p.Cys1517Phe
|
|
XM_011514298.1:c.3962G>T
|
XP_011512600.1:p.Cys1321Phe
|
|
XM_011514299.1:c.4094G>T
|
XP_011512601.1:p.Cys1365Phe
|
|
XM_011514300.1:c.3914G>T
|
XP_011512602.1:p.Cys1305Phe
|
|
XM_011514301.1:c.3851G>T
|
XP_011512603.1:p.Cys1284Phe
|
|
XM_011514302.1:c.3695G>T
|
XP_011512604.1:p.Cys1232Phe
|
|
XM_011514299.2:c.4094G>T
|
XP_011512601.1:p.Cys1365Phe
|
|
XM_011514300.2:c.3914G>T
|
XP_011512602.1:p.Cys1305Phe
|
|
XM_011514302.2:c.3695G>T
|
XP_011512604.1:p.Cys1232Phe
|
|
XM_017010250.1:c.4808G>T
|
XP_016865739.1:p.Cys1603Phe
|
|
XM_017010251.2:c.3626G>T
|
XP_016865740.1:p.Cys1209Phe
|
|
NM_080680.3:c.4808G>T
MANE Select
|
NP_542411.2:p.Cys1603Phe
|
|
NM_080681.3:c.4550G>T
|
NP_542412.2:p.Cys1517Phe
|
|
NM_080679.3:c.4487G>T
|
NP_542410.2:p.Cys1496Phe
|
|