ENST00000389048.8:c.3805G>A
MANE Select
|
ENSP00000373700.3:p.Gly1269Arg
|
|
ENST00000431873.6:c.1032G>A
|
|
|
ENST00000638605.1:n.682G>A
|
|
|
ENST00000642122.1:c.601G>A
|
ENSP00000493203.1:p.Gly201Arg
|
|
ENST00000389048.7:c.3805G>A
|
ENSP00000373700.3:p.Gly1269Arg
|
|
ENST00000431873.5:c.685G>A
|
ENSP00000414027.2:p.Gly229Arg
|
|
ENST00000618119.4:c.2674G>A
|
ENSP00000482733.1:p.Gly892Arg
|
|
NM_004304.4:c.3805G>A
|
NP_004295.2:p.Gly1269Arg
|
|
NM_001353765.1:c.601G>A
|
NP_001340694.1:p.Gly201Arg
|
|
XM_024452778.1:c.958G>A
|
XP_024308546.1:p.Gly320Arg
|
|
XM_024452779.1:c.601G>A
|
XP_024308547.1:p.Gly201Arg
|
|
NM_004304.5:c.3805G>A
MANE Select
|
NP_004295.2:p.Gly1269Arg
|
|
NM_001353765.2:c.601G>A
|
NP_001340694.1:p.Gly201Arg
|
|