ENST00000261937.11:c.4068T>G
MANE Select
|
ENSP00000261937.6:p.Thr1356=
|
|
ENST00000261937.10:c.4068T>G
|
ENSP00000261937.6:p.Thr1356=
|
|
ENST00000502603.5:n.768T>G
|
|
|
NM_182925.4:c.4068T>G
|
NP_891555.2:p.Thr1356=
|
|
XM_011534477.1:c.4317T>G
|
XP_011532779.1:p.Thr1439=
|
|
XM_011534478.1:c.4299T>G
|
XP_011532780.1:p.Thr1433=
|
|
XM_011534482.1:c.4086T>G
|
XP_011532784.1:p.Thr1362=
|
|
XM_011534483.1:c.4008T>G
|
XP_011532785.1:p.Thr1336=
|
|
XM_011534484.1:c.3609T>G
|
XP_011532786.1:p.Thr1203=
|
|
XR_941095.1:n.4354T>G
|
|
|
XM_011534478.3:c.4299T>G
|
XP_011532780.1:p.Thr1433=
|
|
XM_011534484.2:c.3609T>G
|
XP_011532786.1:p.Thr1203=
|
|
XM_017009263.1:c.*214T>G
|
XP_016864752.1:n.*214T>G
|
|
XM_017009268.1:c.3990T>G
|
XP_016864757.1:p.Thr1330=
|
|
XR_001742050.2:n.4558T>G
|
|
|
NM_182925.5:c.4068T>G
MANE Select
|
NP_891555.2:p.Thr1356=
|
|