ENST00000261937.11:c.4066A>G
MANE Select
|
ENSP00000261937.6:p.Thr1356Ala
|
|
ENST00000261937.10:c.4066A>G
|
ENSP00000261937.6:p.Thr1356Ala
|
|
ENST00000502603.5:n.766A>G
|
|
|
NM_182925.4:c.4066A>G
|
NP_891555.2:p.Thr1356Ala
|
|
XM_011534477.1:c.4315A>G
|
XP_011532779.1:p.Thr1439Ala
|
|
XM_011534478.1:c.4297A>G
|
XP_011532780.1:p.Thr1433Ala
|
|
XM_011534482.1:c.4084A>G
|
XP_011532784.1:p.Thr1362Ala
|
|
XM_011534483.1:c.4006A>G
|
XP_011532785.1:p.Thr1336Ala
|
|
XM_011534484.1:c.3607A>G
|
XP_011532786.1:p.Thr1203Ala
|
|
XR_941095.1:n.4352A>G
|
|
|
XM_011534478.3:c.4297A>G
|
XP_011532780.1:p.Thr1433Ala
|
|
XM_011534484.2:c.3607A>G
|
XP_011532786.1:p.Thr1203Ala
|
|
XM_017009263.1:c.*212A>G
|
XP_016864752.1:n.*212A>G
|
|
XM_017009268.1:c.3988A>G
|
XP_016864757.1:p.Thr1330Ala
|
|
XR_001742050.2:n.4556A>G
|
|
|
NM_182925.5:c.4066A>G
MANE Select
|
NP_891555.2:p.Thr1356Ala
|
|