ENST00000260943.11:c.3745C>G
|
ENSP00000260943.7:p.Arg1249Gly
|
|
ENST00000342788.9:c.3823C>G
MANE Select
|
ENSP00000342235.4:p.Arg1275Gly
|
|
ENST00000402597.6:c.3697C>G
|
ENSP00000385565.3:p.Arg1233Gly
|
|
ENST00000342788.8:c.3823C>G
|
ENSP00000342235.4:p.Arg1275Gly
|
|
ENST00000402597.5:c.3646C>G
|
ENSP00000385565.2:p.Arg1216Gly
|
|
ENST00000436443.5:c.3775C>G
|
ENSP00000403204.1:p.Arg1259Gly
|
|
NM_001042599.1:c.3775C>G
|
NP_001036064.1:p.Arg1259Gly
|
|
NM_005235.2:c.3823C>G
|
NP_005226.1:p.Arg1275Gly
|
|
XM_005246375.1:c.3820C>G
|
XP_005246432.1:p.Arg1274Gly
|
|
XM_005246376.1:c.3793C>G
|
XP_005246433.1:p.Arg1265Gly
|
|
XM_005246377.1:c.3745C>G
|
XP_005246434.1:p.Arg1249Gly
|
|
XM_006712364.1:c.3868C>G
|
XP_006712427.1:p.Arg1290Gly
|
|
XM_005246376.3:c.3793C>G
|
XP_005246433.1:p.Arg1265Gly
|
|
XM_005246377.3:c.3745C>G
|
XP_005246434.1:p.Arg1249Gly
|
|
XM_006712364.3:c.3868C>G
|
XP_006712427.1:p.Arg1290Gly
|
|
XM_017003577.2:c.3946C>G
|
XP_016859066.1:p.Arg1316Gly
|
|
XM_017003578.2:c.3901C>G
|
XP_016859067.1:p.Arg1301Gly
|
|
XM_017003579.2:c.3898C>G
|
XP_016859068.1:p.Arg1300Gly
|
|
XM_017003580.2:c.3871C>G
|
XP_016859069.1:p.Arg1291Gly
|
|
XM_017003581.2:c.3853C>G
|
XP_016859070.1:p.Arg1285Gly
|
|
XM_017003582.1:c.3247C>G
|
XP_016859071.1:p.Arg1083Gly
|
|
NM_005235.3:c.3823C>G
MANE Select
|
NP_005226.1:p.Arg1275Gly
|
|