ENST00000261937.11:c.3988C>T
MANE Select
|
ENSP00000261937.6:p.Gln1330Ter
|
|
ENST00000261937.10:c.3988C>T
|
ENSP00000261937.6:p.Gln1330Ter
|
|
ENST00000502603.5:n.688C>T
|
|
|
NM_182925.4:c.3988C>T
|
NP_891555.2:p.Gln1330Ter
|
|
XM_011534477.1:c.4237C>T
|
XP_011532779.1:p.Gln1413Ter
|
|
XM_011534478.1:c.4219C>T
|
XP_011532780.1:p.Gln1407Ter
|
|
XM_011534482.1:c.4006C>T
|
XP_011532784.1:p.Gln1336Ter
|
|
XM_011534483.1:c.3928C>T
|
XP_011532785.1:p.Gln1310Ter
|
|
XM_011534484.1:c.3529C>T
|
XP_011532786.1:p.Gln1177Ter
|
|
XR_941095.1:n.4274C>T
|
|
|
XM_011534478.3:c.4219C>T
|
XP_011532780.1:p.Gln1407Ter
|
|
XM_011534484.2:c.3529C>T
|
XP_011532786.1:p.Gln1177Ter
|
|
XM_017009263.1:c.*134C>T
|
XP_016864752.1:n.*134C>T
|
|
XM_017009268.1:c.3910C>T
|
XP_016864757.1:p.Gln1304Ter
|
|
XR_001742050.2:n.4478C>T
|
|
|
NM_182925.5:c.3988C>T
MANE Select
|
NP_891555.2:p.Gln1330Ter
|
|