ENST00000683572.1:n.776G=
|
|
|
ENST00000341947.7:c.4970G=
MANE Select
|
ENSP00000339915.2:p.Gly1657=
|
|
ENST00000341947.6:c.4970G=
|
ENSP00000339915.2:p.Gly1657=
|
|
ENST00000361917.5:c.4649G=
|
ENSP00000355123.1:p.Gly1550=
|
|
ENST00000374708.8:c.4712G=
|
ENSP00000363840.4:p.Gly1571=
|
|
ENST00000477772.1:n.760G=
|
|
|
NM_080679.2:c.4649G=
|
NP_542410.2:p.Gly1550=
|
|
NM_080680.2:c.4970G=
|
NP_542411.2:p.Gly1657=
|
|
NM_080681.2:c.4712G=
|
NP_542412.2:p.Gly1571=
|
|
XM_011514298.1:c.4124G=
|
XP_011512600.1:p.Gly1375=
|
|
XM_011514299.1:c.4256G=
|
XP_011512601.1:p.Gly1419=
|
|
XM_011514300.1:c.4076G=
|
XP_011512602.1:p.Gly1359=
|
|
XM_011514301.1:c.4013G=
|
XP_011512603.1:p.Gly1338=
|
|
XM_011514302.1:c.3857G=
|
XP_011512604.1:p.Gly1286=
|
|
XM_011514299.2:c.4256G=
|
XP_011512601.1:p.Gly1419=
|
|
XM_011514300.2:c.4076G=
|
XP_011512602.1:p.Gly1359=
|
|
XM_011514302.2:c.3857G=
|
XP_011512604.1:p.Gly1286=
|
|
XM_017010250.1:c.4970G=
|
XP_016865739.1:p.Gly1657=
|
|
XM_017010251.2:c.3788G=
|
XP_016865740.1:p.Gly1263=
|
|
NM_080680.3:c.4970G=
MANE Select
|
NP_542411.2:p.Gly1657=
|
|
NM_080681.3:c.4712G=
|
NP_542412.2:p.Gly1571=
|
|
NM_080679.3:c.4649G=
|
NP_542410.2:p.Gly1550=
|
|