ENST00000683572.1:n.773C>A
|
|
|
ENST00000341947.7:c.4967C>A
MANE Select
|
ENSP00000339915.2:p.Ser1656Tyr
|
|
ENST00000341947.6:c.4967C>A
|
ENSP00000339915.2:p.Ser1656Tyr
|
|
ENST00000361917.5:c.4646C>A
|
ENSP00000355123.1:p.Ser1549Tyr
|
|
ENST00000374708.8:c.4709C>A
|
ENSP00000363840.4:p.Ser1570Tyr
|
|
ENST00000477772.1:n.757C>A
|
|
|
NM_080679.2:c.4646C>A
|
NP_542410.2:p.Ser1549Tyr
|
|
NM_080680.2:c.4967C>A
|
NP_542411.2:p.Ser1656Tyr
|
|
NM_080681.2:c.4709C>A
|
NP_542412.2:p.Ser1570Tyr
|
|
XM_011514298.1:c.4121C>A
|
XP_011512600.1:p.Ser1374Tyr
|
|
XM_011514299.1:c.4253C>A
|
XP_011512601.1:p.Ser1418Tyr
|
|
XM_011514300.1:c.4073C>A
|
XP_011512602.1:p.Ser1358Tyr
|
|
XM_011514301.1:c.4010C>A
|
XP_011512603.1:p.Ser1337Tyr
|
|
XM_011514302.1:c.3854C>A
|
XP_011512604.1:p.Ser1285Tyr
|
|
XM_011514299.2:c.4253C>A
|
XP_011512601.1:p.Ser1418Tyr
|
|
XM_011514300.2:c.4073C>A
|
XP_011512602.1:p.Ser1358Tyr
|
|
XM_011514302.2:c.3854C>A
|
XP_011512604.1:p.Ser1285Tyr
|
|
XM_017010250.1:c.4967C>A
|
XP_016865739.1:p.Ser1656Tyr
|
|
XM_017010251.2:c.3785C>A
|
XP_016865740.1:p.Ser1262Tyr
|
|
NM_080680.3:c.4967C>A
MANE Select
|
NP_542411.2:p.Ser1656Tyr
|
|
NM_080681.3:c.4709C>A
|
NP_542412.2:p.Ser1570Tyr
|
|
NM_080679.3:c.4646C>A
|
NP_542410.2:p.Ser1549Tyr
|
|