ENST00000403733.8:c.3177G>A
MANE Select
|
ENSP00000384222.3:p.Gln1059=
|
|
ENST00000403733.7:c.3177G>A
|
ENSP00000384222.3:p.Gln1059=
|
|
ENST00000427431.5:c.*2569G>A
|
ENSP00000393342.1:n.*2569G>A
|
|
ENST00000438543.5:c.*973G>A
|
ENSP00000413521.1:n.*973G>A
|
|
ENST00000448232.6:c.3249G>A
|
ENSP00000398577.2:p.Gln1083=
|
|
ENST00000504005.5:c.2223G>A
|
ENSP00000427569.1:p.Gln741=
|
|
ENST00000508747.1:c.561G>A
|
ENSP00000420835.1:p.Gln187=
|
|
ENST00000513834.5:c.3030G>A
|
ENSP00000425054.1:p.Gln1010=
|
|
NM_024949.5:c.3177G>A
|
NP_079225.5:p.Gln1059=
|
|
XM_011532269.1:c.3249G>A
|
XP_011530571.1:p.Gln1083=
|
|
XM_011532269.3:c.3249G>A
|
XP_011530571.1:p.Gln1083=
|
|
XM_024454225.1:c.2955G>A
|
XP_024309993.1:p.Gln985=
|
|
NM_024949.6:c.3177G>A
MANE Select
|
NP_079225.5:p.Gln1059=
|
|