ENST00000683572.1:n.583G=
|
|
|
ENST00000341947.7:c.4777G=
MANE Select
|
ENSP00000339915.2:p.Gly1593=
|
|
ENST00000341947.6:c.4777G=
|
ENSP00000339915.2:p.Gly1593=
|
|
ENST00000361917.5:c.4456G=
|
ENSP00000355123.1:p.Gly1486=
|
|
ENST00000374708.8:c.4519G=
|
ENSP00000363840.4:p.Gly1507=
|
|
ENST00000477772.1:n.567G=
|
|
|
NM_080679.2:c.4456G=
|
NP_542410.2:p.Gly1486=
|
|
NM_080680.2:c.4777G=
|
NP_542411.2:p.Gly1593=
|
|
NM_080681.2:c.4519G=
|
NP_542412.2:p.Gly1507=
|
|
XM_011514298.1:c.3931G=
|
XP_011512600.1:p.Gly1311=
|
|
XM_011514299.1:c.4063G=
|
XP_011512601.1:p.Gly1355=
|
|
XM_011514300.1:c.3883G=
|
XP_011512602.1:p.Gly1295=
|
|
XM_011514301.1:c.3820G=
|
XP_011512603.1:p.Gly1274=
|
|
XM_011514302.1:c.3664G=
|
XP_011512604.1:p.Gly1222=
|
|
XM_011514299.2:c.4063G=
|
XP_011512601.1:p.Gly1355=
|
|
XM_011514300.2:c.3883G=
|
XP_011512602.1:p.Gly1295=
|
|
XM_011514302.2:c.3664G=
|
XP_011512604.1:p.Gly1222=
|
|
XM_017010250.1:c.4777G=
|
XP_016865739.1:p.Gly1593=
|
|
XM_017010251.2:c.3595G=
|
XP_016865740.1:p.Gly1199=
|
|
NM_080680.3:c.4777G=
MANE Select
|
NP_542411.2:p.Gly1593=
|
|
NM_080681.3:c.4519G=
|
NP_542412.2:p.Gly1507=
|
|
NM_080679.3:c.4456G=
|
NP_542410.2:p.Gly1486=
|
|