ENST00000683572.1:n.621C>T
|
|
|
ENST00000341947.7:c.4815C>T
MANE Select
|
ENSP00000339915.2:p.Phe1605=
|
|
ENST00000341947.6:c.4815C>T
|
ENSP00000339915.2:p.Phe1605=
|
|
ENST00000361917.5:c.4494C>T
|
ENSP00000355123.1:p.Phe1498=
|
|
ENST00000374708.8:c.4557C>T
|
ENSP00000363840.4:p.Phe1519=
|
|
ENST00000477772.1:n.605C>T
|
|
|
NM_080679.2:c.4494C>T
|
NP_542410.2:p.Phe1498=
|
|
NM_080680.2:c.4815C>T
|
NP_542411.2:p.Phe1605=
|
|
NM_080681.2:c.4557C>T
|
NP_542412.2:p.Phe1519=
|
|
XM_011514298.1:c.3969C>T
|
XP_011512600.1:p.Phe1323=
|
|
XM_011514299.1:c.4101C>T
|
XP_011512601.1:p.Phe1367=
|
|
XM_011514300.1:c.3921C>T
|
XP_011512602.1:p.Phe1307=
|
|
XM_011514301.1:c.3858C>T
|
XP_011512603.1:p.Phe1286=
|
|
XM_011514302.1:c.3702C>T
|
XP_011512604.1:p.Phe1234=
|
|
XM_011514299.2:c.4101C>T
|
XP_011512601.1:p.Phe1367=
|
|
XM_011514300.2:c.3921C>T
|
XP_011512602.1:p.Phe1307=
|
|
XM_011514302.2:c.3702C>T
|
XP_011512604.1:p.Phe1234=
|
|
XM_017010250.1:c.4815C>T
|
XP_016865739.1:p.Phe1605=
|
|
XM_017010251.2:c.3633C>T
|
XP_016865740.1:p.Phe1211=
|
|
NM_080680.3:c.4815C>T
MANE Select
|
NP_542411.2:p.Phe1605=
|
|
NM_080681.3:c.4557C>T
|
NP_542412.2:p.Phe1519=
|
|
NM_080679.3:c.4494C>T
|
NP_542410.2:p.Phe1498=
|
|