ENST00000261937.11:c.3903A>G
MANE Select
|
ENSP00000261937.6:p.Gly1301=
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ENST00000261937.10:c.3903A>G
|
ENSP00000261937.6:p.Gly1301=
|
|
ENST00000502603.5:n.603A>G
|
|
|
NM_182925.4:c.3903A>G
|
NP_891555.2:p.Gly1301=
|
|
XM_011534477.1:c.4152A>G
|
XP_011532779.1:p.Gly1384=
|
|
XM_011534478.1:c.4134A>G
|
XP_011532780.1:p.Gly1378=
|
|
XM_011534479.1:c.*49A>G
|
XP_011532781.1:n.*49A>G
|
|
XM_011534482.1:c.3921A>G
|
XP_011532784.1:p.Gly1307=
|
|
XM_011534483.1:c.3843A>G
|
XP_011532785.1:p.Gly1281=
|
|
XM_011534484.1:c.3444A>G
|
XP_011532786.1:p.Gly1148=
|
|
XR_941095.1:n.4189A>G
|
|
|
XM_011534478.3:c.4134A>G
|
XP_011532780.1:p.Gly1378=
|
|
XM_011534484.2:c.3444A>G
|
XP_011532786.1:p.Gly1148=
|
|
XM_017009263.1:c.*49A>G
|
XP_016864752.1:n.*49A>G
|
|
XM_017009268.1:c.3825A>G
|
XP_016864757.1:p.Gly1275=
|
|
XR_001742050.2:n.4393A>G
|
|
|
NM_182925.5:c.3903A>G
MANE Select
|
NP_891555.2:p.Gly1301=
|
|