ENST00000683572.1:n.630G=
|
|
|
ENST00000341947.7:c.4824G=
MANE Select
|
ENSP00000339915.2:p.Gly1608=
|
|
ENST00000341947.6:c.4824G=
|
ENSP00000339915.2:p.Gly1608=
|
|
ENST00000361917.5:c.4503G=
|
ENSP00000355123.1:p.Gly1501=
|
|
ENST00000374708.8:c.4566G=
|
ENSP00000363840.4:p.Gly1522=
|
|
ENST00000477772.1:n.614G=
|
|
|
NM_080679.2:c.4503G=
|
NP_542410.2:p.Gly1501=
|
|
NM_080680.2:c.4824G=
|
NP_542411.2:p.Gly1608=
|
|
NM_080681.2:c.4566G=
|
NP_542412.2:p.Gly1522=
|
|
XM_011514298.1:c.3978G=
|
XP_011512600.1:p.Gly1326=
|
|
XM_011514299.1:c.4110G=
|
XP_011512601.1:p.Gly1370=
|
|
XM_011514300.1:c.3930G=
|
XP_011512602.1:p.Gly1310=
|
|
XM_011514301.1:c.3867G=
|
XP_011512603.1:p.Gly1289=
|
|
XM_011514302.1:c.3711G=
|
XP_011512604.1:p.Gly1237=
|
|
XM_011514299.2:c.4110G=
|
XP_011512601.1:p.Gly1370=
|
|
XM_011514300.2:c.3930G=
|
XP_011512602.1:p.Gly1310=
|
|
XM_011514302.2:c.3711G=
|
XP_011512604.1:p.Gly1237=
|
|
XM_017010250.1:c.4824G=
|
XP_016865739.1:p.Gly1608=
|
|
XM_017010251.2:c.3642G=
|
XP_016865740.1:p.Gly1214=
|
|
NM_080680.3:c.4824G=
MANE Select
|
NP_542411.2:p.Gly1608=
|
|
NM_080681.3:c.4566G=
|
NP_542412.2:p.Gly1522=
|
|
NM_080679.3:c.4503G=
|
NP_542410.2:p.Gly1501=
|
|