ENST00000261937.11:c.3911A>G
MANE Select
|
ENSP00000261937.6:p.Gln1304Arg
|
|
ENST00000261937.10:c.3911A>G
|
ENSP00000261937.6:p.Gln1304Arg
|
|
ENST00000502603.5:n.611A>G
|
|
|
NM_182925.4:c.3911A>G
|
NP_891555.2:p.Gln1304Arg
|
|
XM_011534477.1:c.4160A>G
|
XP_011532779.1:p.Gln1387Arg
|
|
XM_011534478.1:c.4142A>G
|
XP_011532780.1:p.Gln1381Arg
|
|
XM_011534479.1:c.*57A>G
|
XP_011532781.1:n.*57A>G
|
|
XM_011534482.1:c.3929A>G
|
XP_011532784.1:p.Gln1310Arg
|
|
XM_011534483.1:c.3851A>G
|
XP_011532785.1:p.Gln1284Arg
|
|
XM_011534484.1:c.3452A>G
|
XP_011532786.1:p.Gln1151Arg
|
|
XR_941095.1:n.4197A>G
|
|
|
XM_011534478.3:c.4142A>G
|
XP_011532780.1:p.Gln1381Arg
|
|
XM_011534484.2:c.3452A>G
|
XP_011532786.1:p.Gln1151Arg
|
|
XM_017009263.1:c.*57A>G
|
XP_016864752.1:n.*57A>G
|
|
XM_017009268.1:c.3833A>G
|
XP_016864757.1:p.Gln1278Arg
|
|
XR_001742050.2:n.4401A>G
|
|
|
NM_182925.5:c.3911A>G
MANE Select
|
NP_891555.2:p.Gln1304Arg
|
|