ENST00000683572.1:n.686C>A
|
|
|
ENST00000341947.7:c.4880C>A
MANE Select
|
ENSP00000339915.2:p.Ser1627Ter
|
|
ENST00000341947.6:c.4880C>A
|
ENSP00000339915.2:p.Ser1627Ter
|
|
ENST00000361917.5:c.4559C>A
|
ENSP00000355123.1:p.Ser1520Ter
|
|
ENST00000374708.8:c.4622C>A
|
ENSP00000363840.4:p.Ser1541Ter
|
|
ENST00000477772.1:n.670C>A
|
|
|
NM_080679.2:c.4559C>A
|
NP_542410.2:p.Ser1520Ter
|
|
NM_080680.2:c.4880C>A
|
NP_542411.2:p.Ser1627Ter
|
|
NM_080681.2:c.4622C>A
|
NP_542412.2:p.Ser1541Ter
|
|
XM_011514298.1:c.4034C>A
|
XP_011512600.1:p.Ser1345Ter
|
|
XM_011514299.1:c.4166C>A
|
XP_011512601.1:p.Ser1389Ter
|
|
XM_011514300.1:c.3986C>A
|
XP_011512602.1:p.Ser1329Ter
|
|
XM_011514301.1:c.3923C>A
|
XP_011512603.1:p.Ser1308Ter
|
|
XM_011514302.1:c.3767C>A
|
XP_011512604.1:p.Ser1256Ter
|
|
XM_011514299.2:c.4166C>A
|
XP_011512601.1:p.Ser1389Ter
|
|
XM_011514300.2:c.3986C>A
|
XP_011512602.1:p.Ser1329Ter
|
|
XM_011514302.2:c.3767C>A
|
XP_011512604.1:p.Ser1256Ter
|
|
XM_017010250.1:c.4880C>A
|
XP_016865739.1:p.Ser1627Ter
|
|
XM_017010251.2:c.3698C>A
|
XP_016865740.1:p.Ser1233Ter
|
|
NM_080680.3:c.4880C>A
MANE Select
|
NP_542411.2:p.Ser1627Ter
|
|
NM_080681.3:c.4622C>A
|
NP_542412.2:p.Ser1541Ter
|
|
NM_080679.3:c.4559C>A
|
NP_542410.2:p.Ser1520Ter
|
|