ENST00000341947.7:c.3100C>G
MANE Select
|
ENSP00000339915.2:p.Arg1034Gly
|
|
ENST00000341947.6:c.3100C>G
|
ENSP00000339915.2:p.Arg1034Gly
|
|
ENST00000361917.5:c.2779C>G
|
ENSP00000355123.1:p.Arg927Gly
|
|
ENST00000374708.8:c.2842C>G
|
ENSP00000363840.4:p.Arg948Gly
|
|
ENST00000477772.1:n.272+5246C>G
|
|
|
NM_080679.2:c.2779C>G
|
NP_542410.2:p.Arg927Gly
|
|
NM_080680.2:c.3100C>G
|
NP_542411.2:p.Arg1034Gly
|
|
NM_080681.2:c.2842C>G
|
NP_542412.2:p.Arg948Gly
|
|
XM_011514298.1:c.2254C>G
|
XP_011512600.1:p.Arg752Gly
|
|
XM_011514299.1:c.2386C>G
|
XP_011512601.1:p.Arg796Gly
|
|
XM_011514300.1:c.2206C>G
|
XP_011512602.1:p.Arg736Gly
|
|
XM_011514301.1:c.2143C>G
|
XP_011512603.1:p.Arg715Gly
|
|
XM_011514302.1:c.1987C>G
|
XP_011512604.1:p.Arg663Gly
|
|
XM_011514299.2:c.2386C>G
|
XP_011512601.1:p.Arg796Gly
|
|
XM_011514300.2:c.2206C>G
|
XP_011512602.1:p.Arg736Gly
|
|
XM_011514302.2:c.1987C>G
|
XP_011512604.1:p.Arg663Gly
|
|
XM_017010250.1:c.3100C>G
|
XP_016865739.1:p.Arg1034Gly
|
|
XM_017010251.2:c.1918C>G
|
XP_016865740.1:p.Arg640Gly
|
|
NM_080680.3:c.3100C>G
MANE Select
|
NP_542411.2:p.Arg1034Gly
|
|
NM_080681.3:c.2842C>G
|
NP_542412.2:p.Arg948Gly
|
|
NM_080679.3:c.2779C>G
|
NP_542410.2:p.Arg927Gly
|
|