ENST00000261937.11:c.3982G>C
MANE Select
|
ENSP00000261937.6:p.Gly1328Arg
|
|
ENST00000261937.10:c.3982G>C
|
ENSP00000261937.6:p.Gly1328Arg
|
|
ENST00000502603.5:n.682G>C
|
|
|
NM_182925.4:c.3982G>C
|
NP_891555.2:p.Gly1328Arg
|
|
XM_011534477.1:c.4231G>C
|
XP_011532779.1:p.Gly1411Arg
|
|
XM_011534478.1:c.4213G>C
|
XP_011532780.1:p.Gly1405Arg
|
|
XM_011534482.1:c.4000G>C
|
XP_011532784.1:p.Gly1334Arg
|
|
XM_011534483.1:c.3922G>C
|
XP_011532785.1:p.Gly1308Arg
|
|
XM_011534484.1:c.3523G>C
|
XP_011532786.1:p.Gly1175Arg
|
|
XR_941095.1:n.4268G>C
|
|
|
XM_011534478.3:c.4213G>C
|
XP_011532780.1:p.Gly1405Arg
|
|
XM_011534484.2:c.3523G>C
|
XP_011532786.1:p.Gly1175Arg
|
|
XM_017009263.1:c.*128G>C
|
XP_016864752.1:n.*128G>C
|
|
XM_017009268.1:c.3904G>C
|
XP_016864757.1:p.Gly1302Arg
|
|
XR_001742050.2:n.4472G>C
|
|
|
NM_182925.5:c.3982G>C
MANE Select
|
NP_891555.2:p.Gly1328Arg
|
|