ENST00000261937.11:c.4069T>G
MANE Select
|
ENSP00000261937.6:p.Phe1357Val
|
|
ENST00000261937.10:c.4069T>G
|
ENSP00000261937.6:p.Phe1357Val
|
|
ENST00000502603.5:n.769T>G
|
|
|
NM_182925.4:c.4069T>G
|
NP_891555.2:p.Phe1357Val
|
|
XM_011534477.1:c.4318T>G
|
XP_011532779.1:p.Phe1440Val
|
|
XM_011534478.1:c.4300T>G
|
XP_011532780.1:p.Phe1434Val
|
|
XM_011534482.1:c.4087T>G
|
XP_011532784.1:p.Phe1363Val
|
|
XM_011534483.1:c.4009T>G
|
XP_011532785.1:p.Phe1337Val
|
|
XM_011534484.1:c.3610T>G
|
XP_011532786.1:p.Phe1204Val
|
|
XR_941095.1:n.4355T>G
|
|
|
XM_011534478.3:c.4300T>G
|
XP_011532780.1:p.Phe1434Val
|
|
XM_011534484.2:c.3610T>G
|
XP_011532786.1:p.Phe1204Val
|
|
XM_017009263.1:c.*215T>G
|
XP_016864752.1:n.*215T>G
|
|
XM_017009268.1:c.3991T>G
|
XP_016864757.1:p.Phe1331Val
|
|
XR_001742050.2:n.4559T>G
|
|
|
NM_182925.5:c.4069T>G
MANE Select
|
NP_891555.2:p.Phe1357Val
|
|