ENST00000683572.1:n.694T>G
|
|
|
ENST00000341947.7:c.4888T>G
MANE Select
|
ENSP00000339915.2:p.Ser1630Ala
|
|
ENST00000341947.6:c.4888T>G
|
ENSP00000339915.2:p.Ser1630Ala
|
|
ENST00000361917.5:c.4567T>G
|
ENSP00000355123.1:p.Ser1523Ala
|
|
ENST00000374708.8:c.4630T>G
|
ENSP00000363840.4:p.Ser1544Ala
|
|
ENST00000477772.1:n.678T>G
|
|
|
NM_080679.2:c.4567T>G
|
NP_542410.2:p.Ser1523Ala
|
|
NM_080680.2:c.4888T>G
|
NP_542411.2:p.Ser1630Ala
|
|
NM_080681.2:c.4630T>G
|
NP_542412.2:p.Ser1544Ala
|
|
XM_011514298.1:c.4042T>G
|
XP_011512600.1:p.Ser1348Ala
|
|
XM_011514299.1:c.4174T>G
|
XP_011512601.1:p.Ser1392Ala
|
|
XM_011514300.1:c.3994T>G
|
XP_011512602.1:p.Ser1332Ala
|
|
XM_011514301.1:c.3931T>G
|
XP_011512603.1:p.Ser1311Ala
|
|
XM_011514302.1:c.3775T>G
|
XP_011512604.1:p.Ser1259Ala
|
|
XM_011514299.2:c.4174T>G
|
XP_011512601.1:p.Ser1392Ala
|
|
XM_011514300.2:c.3994T>G
|
XP_011512602.1:p.Ser1332Ala
|
|
XM_011514302.2:c.3775T>G
|
XP_011512604.1:p.Ser1259Ala
|
|
XM_017010250.1:c.4888T>G
|
XP_016865739.1:p.Ser1630Ala
|
|
XM_017010251.2:c.3706T>G
|
XP_016865740.1:p.Ser1236Ala
|
|
NM_080680.3:c.4888T>G
MANE Select
|
NP_542411.2:p.Ser1630Ala
|
|
NM_080681.3:c.4630T>G
|
NP_542412.2:p.Ser1544Ala
|
|
NM_080679.3:c.4567T>G
|
NP_542410.2:p.Ser1523Ala
|
|