ENST00000683572.1:n.691G>A
|
|
|
ENST00000341947.7:c.4885G>A
MANE Select
|
ENSP00000339915.2:p.Gly1629Ser
|
|
ENST00000341947.6:c.4885G>A
|
ENSP00000339915.2:p.Gly1629Ser
|
|
ENST00000361917.5:c.4564G>A
|
ENSP00000355123.1:p.Gly1522Ser
|
|
ENST00000374708.8:c.4627G>A
|
ENSP00000363840.4:p.Gly1543Ser
|
|
ENST00000477772.1:n.675G>A
|
|
|
NM_080679.2:c.4564G>A
|
NP_542410.2:p.Gly1522Ser
|
|
NM_080680.2:c.4885G>A
|
NP_542411.2:p.Gly1629Ser
|
|
NM_080681.2:c.4627G>A
|
NP_542412.2:p.Gly1543Ser
|
|
XM_011514298.1:c.4039G>A
|
XP_011512600.1:p.Gly1347Ser
|
|
XM_011514299.1:c.4171G>A
|
XP_011512601.1:p.Gly1391Ser
|
|
XM_011514300.1:c.3991G>A
|
XP_011512602.1:p.Gly1331Ser
|
|
XM_011514301.1:c.3928G>A
|
XP_011512603.1:p.Gly1310Ser
|
|
XM_011514302.1:c.3772G>A
|
XP_011512604.1:p.Gly1258Ser
|
|
XM_011514299.2:c.4171G>A
|
XP_011512601.1:p.Gly1391Ser
|
|
XM_011514300.2:c.3991G>A
|
XP_011512602.1:p.Gly1331Ser
|
|
XM_011514302.2:c.3772G>A
|
XP_011512604.1:p.Gly1258Ser
|
|
XM_017010250.1:c.4885G>A
|
XP_016865739.1:p.Gly1629Ser
|
|
XM_017010251.2:c.3703G>A
|
XP_016865740.1:p.Gly1235Ser
|
|
NM_080680.3:c.4885G>A
MANE Select
|
NP_542411.2:p.Gly1629Ser
|
|
NM_080681.3:c.4627G>A
|
NP_542412.2:p.Gly1543Ser
|
|
NM_080679.3:c.4564G>A
|
NP_542410.2:p.Gly1522Ser
|
|