ENST00000261937.11:c.4079A>G
MANE Select
|
ENSP00000261937.6:p.Asp1360Gly
|
|
ENST00000261937.10:c.4079A>G
|
ENSP00000261937.6:p.Asp1360Gly
|
|
ENST00000502603.5:n.779A>G
|
|
|
NM_182925.4:c.4079A>G
|
NP_891555.2:p.Asp1360Gly
|
|
XM_011534477.1:c.4328A>G
|
XP_011532779.1:p.Asp1443Gly
|
|
XM_011534478.1:c.4310A>G
|
XP_011532780.1:p.Asp1437Gly
|
|
XM_011534482.1:c.4097A>G
|
XP_011532784.1:p.Asp1366Gly
|
|
XM_011534483.1:c.4019A>G
|
XP_011532785.1:p.Asp1340Gly
|
|
XM_011534484.1:c.3620A>G
|
XP_011532786.1:p.Asp1207Gly
|
|
XR_941095.1:n.4365A>G
|
|
|
XM_011534478.3:c.4310A>G
|
XP_011532780.1:p.Asp1437Gly
|
|
XM_011534484.2:c.3620A>G
|
XP_011532786.1:p.Asp1207Gly
|
|
XM_017009263.1:c.*225A>G
|
XP_016864752.1:n.*225A>G
|
|
XM_017009268.1:c.4001A>G
|
XP_016864757.1:p.Asp1334Gly
|
|
XR_001742050.2:n.4569A>G
|
|
|
NM_182925.5:c.4079A>G
MANE Select
|
NP_891555.2:p.Asp1360Gly
|
|