ENST00000683572.1:n.692G>A
|
|
|
ENST00000341947.7:c.4886G>A
MANE Select
|
ENSP00000339915.2:p.Gly1629Asp
|
|
ENST00000341947.6:c.4886G>A
|
ENSP00000339915.2:p.Gly1629Asp
|
|
ENST00000361917.5:c.4565G>A
|
ENSP00000355123.1:p.Gly1522Asp
|
|
ENST00000374708.8:c.4628G>A
|
ENSP00000363840.4:p.Gly1543Asp
|
|
ENST00000477772.1:n.676G>A
|
|
|
NM_080679.2:c.4565G>A
|
NP_542410.2:p.Gly1522Asp
|
|
NM_080680.2:c.4886G>A
|
NP_542411.2:p.Gly1629Asp
|
|
NM_080681.2:c.4628G>A
|
NP_542412.2:p.Gly1543Asp
|
|
XM_011514298.1:c.4040G>A
|
XP_011512600.1:p.Gly1347Asp
|
|
XM_011514299.1:c.4172G>A
|
XP_011512601.1:p.Gly1391Asp
|
|
XM_011514300.1:c.3992G>A
|
XP_011512602.1:p.Gly1331Asp
|
|
XM_011514301.1:c.3929G>A
|
XP_011512603.1:p.Gly1310Asp
|
|
XM_011514302.1:c.3773G>A
|
XP_011512604.1:p.Gly1258Asp
|
|
XM_011514299.2:c.4172G>A
|
XP_011512601.1:p.Gly1391Asp
|
|
XM_011514300.2:c.3992G>A
|
XP_011512602.1:p.Gly1331Asp
|
|
XM_011514302.2:c.3773G>A
|
XP_011512604.1:p.Gly1258Asp
|
|
XM_017010250.1:c.4886G>A
|
XP_016865739.1:p.Gly1629Asp
|
|
XM_017010251.2:c.3704G>A
|
XP_016865740.1:p.Gly1235Asp
|
|
NM_080680.3:c.4886G>A
MANE Select
|
NP_542411.2:p.Gly1629Asp
|
|
NM_080681.3:c.4628G>A
|
NP_542412.2:p.Gly1543Asp
|
|
NM_080679.3:c.4565G>A
|
NP_542410.2:p.Gly1522Asp
|
|