ENST00000683572.1:n.687A>T
|
|
|
ENST00000341947.7:c.4881A>T
MANE Select
|
ENSP00000339915.2:p.Ser1627=
|
|
ENST00000341947.6:c.4881A>T
|
ENSP00000339915.2:p.Ser1627=
|
|
ENST00000361917.5:c.4560A>T
|
ENSP00000355123.1:p.Ser1520=
|
|
ENST00000374708.8:c.4623A>T
|
ENSP00000363840.4:p.Ser1541=
|
|
ENST00000477772.1:n.671A>T
|
|
|
NM_080679.2:c.4560A>T
|
NP_542410.2:p.Ser1520=
|
|
NM_080680.2:c.4881A>T
|
NP_542411.2:p.Ser1627=
|
|
NM_080681.2:c.4623A>T
|
NP_542412.2:p.Ser1541=
|
|
XM_011514298.1:c.4035A>T
|
XP_011512600.1:p.Ser1345=
|
|
XM_011514299.1:c.4167A>T
|
XP_011512601.1:p.Ser1389=
|
|
XM_011514300.1:c.3987A>T
|
XP_011512602.1:p.Ser1329=
|
|
XM_011514301.1:c.3924A>T
|
XP_011512603.1:p.Ser1308=
|
|
XM_011514302.1:c.3768A>T
|
XP_011512604.1:p.Ser1256=
|
|
XM_011514299.2:c.4167A>T
|
XP_011512601.1:p.Ser1389=
|
|
XM_011514300.2:c.3987A>T
|
XP_011512602.1:p.Ser1329=
|
|
XM_011514302.2:c.3768A>T
|
XP_011512604.1:p.Ser1256=
|
|
XM_017010250.1:c.4881A>T
|
XP_016865739.1:p.Ser1627=
|
|
XM_017010251.2:c.3699A>T
|
XP_016865740.1:p.Ser1233=
|
|
NM_080680.3:c.4881A>T
MANE Select
|
NP_542411.2:p.Ser1627=
|
|
NM_080681.3:c.4623A>T
|
NP_542412.2:p.Ser1541=
|
|
NM_080679.3:c.4560A>T
|
NP_542410.2:p.Ser1520=
|
|