ENST00000683572.1:n.631G=
|
|
|
ENST00000341947.7:c.4825G=
MANE Select
|
ENSP00000339915.2:p.Gly1609=
|
|
ENST00000341947.6:c.4825G=
|
ENSP00000339915.2:p.Gly1609=
|
|
ENST00000361917.5:c.4504G=
|
ENSP00000355123.1:p.Gly1502=
|
|
ENST00000374708.8:c.4567G=
|
ENSP00000363840.4:p.Gly1523=
|
|
ENST00000477772.1:n.615G=
|
|
|
NM_080679.2:c.4504G=
|
NP_542410.2:p.Gly1502=
|
|
NM_080680.2:c.4825G=
|
NP_542411.2:p.Gly1609=
|
|
NM_080681.2:c.4567G=
|
NP_542412.2:p.Gly1523=
|
|
XM_011514298.1:c.3979G=
|
XP_011512600.1:p.Gly1327=
|
|
XM_011514299.1:c.4111G=
|
XP_011512601.1:p.Gly1371=
|
|
XM_011514300.1:c.3931G=
|
XP_011512602.1:p.Gly1311=
|
|
XM_011514301.1:c.3868G=
|
XP_011512603.1:p.Gly1290=
|
|
XM_011514302.1:c.3712G=
|
XP_011512604.1:p.Gly1238=
|
|
XM_011514299.2:c.4111G=
|
XP_011512601.1:p.Gly1371=
|
|
XM_011514300.2:c.3931G=
|
XP_011512602.1:p.Gly1311=
|
|
XM_011514302.2:c.3712G=
|
XP_011512604.1:p.Gly1238=
|
|
XM_017010250.1:c.4825G=
|
XP_016865739.1:p.Gly1609=
|
|
XM_017010251.2:c.3643G=
|
XP_016865740.1:p.Gly1215=
|
|
NM_080680.3:c.4825G=
MANE Select
|
NP_542411.2:p.Gly1609=
|
|
NM_080681.3:c.4567G=
|
NP_542412.2:p.Gly1523=
|
|
NM_080679.3:c.4504G=
|
NP_542410.2:p.Gly1502=
|
|