ENST00000261937.11:c.3994T>G
MANE Select
|
ENSP00000261937.6:p.Phe1332Val
|
|
ENST00000261937.10:c.3994T>G
|
ENSP00000261937.6:p.Phe1332Val
|
|
ENST00000502603.5:n.694T>G
|
|
|
NM_182925.4:c.3994T>G
|
NP_891555.2:p.Phe1332Val
|
|
XM_011534477.1:c.4243T>G
|
XP_011532779.1:p.Phe1415Val
|
|
XM_011534478.1:c.4225T>G
|
XP_011532780.1:p.Phe1409Val
|
|
XM_011534482.1:c.4012T>G
|
XP_011532784.1:p.Phe1338Val
|
|
XM_011534483.1:c.3934T>G
|
XP_011532785.1:p.Phe1312Val
|
|
XM_011534484.1:c.3535T>G
|
XP_011532786.1:p.Phe1179Val
|
|
XR_941095.1:n.4280T>G
|
|
|
XM_011534478.3:c.4225T>G
|
XP_011532780.1:p.Phe1409Val
|
|
XM_011534484.2:c.3535T>G
|
XP_011532786.1:p.Phe1179Val
|
|
XM_017009263.1:c.*140T>G
|
XP_016864752.1:n.*140T>G
|
|
XM_017009268.1:c.3916T>G
|
XP_016864757.1:p.Phe1306Val
|
|
XR_001742050.2:n.4484T>G
|
|
|
NM_182925.5:c.3994T>G
MANE Select
|
NP_891555.2:p.Phe1332Val
|
|