ENST00000373275.5:c.448A>G
MANE Select
|
ENSP00000362372.4:p.Arg150Gly
|
|
ENST00000373275.4:c.448A>G
|
ENSP00000362372.4:p.Arg150Gly
|
|
ENST00000478415.1:n.660A>G
|
|
|
NM_153252.4:c.448A>G
|
NP_694984.4:p.Arg150Gly
|
|
XM_005262113.2:c.448A>G
|
XP_005262170.1:p.Arg150Gly
|
|
XM_011530903.1:c.-66A>G
|
XP_011529205.1:n.-66A>G
|
|
XM_011530904.1:c.-889A>G
|
XP_011529206.1:n.-889A>G
|
|
XR_430519.2:n.711A>G
|
|
|
XM_005262113.3:c.448A>G
|
XP_005262170.1:p.Arg150Gly
|
|
XM_017029384.1:c.-889A>G
|
XP_016884873.1:n.-889A>G
|
|
XM_017029385.2:c.448A>G
|
XP_016884874.1:p.Arg150Gly
|
|
XR_430519.3:n.713A>G
|
|
|
NM_153252.5:c.448A>G
MANE Select
|
NP_694984.5:p.Arg150Gly
|
|