ENST00000261937.11:c.3998A>G
MANE Select
|
ENSP00000261937.6:p.Tyr1333Cys
|
|
ENST00000261937.10:c.3998A>G
|
ENSP00000261937.6:p.Tyr1333Cys
|
|
ENST00000502603.5:n.698A>G
|
|
|
NM_182925.4:c.3998A>G
|
NP_891555.2:p.Tyr1333Cys
|
|
XM_011534477.1:c.4247A>G
|
XP_011532779.1:p.Tyr1416Cys
|
|
XM_011534478.1:c.4229A>G
|
XP_011532780.1:p.Tyr1410Cys
|
|
XM_011534482.1:c.4016A>G
|
XP_011532784.1:p.Tyr1339Cys
|
|
XM_011534483.1:c.3938A>G
|
XP_011532785.1:p.Tyr1313Cys
|
|
XM_011534484.1:c.3539A>G
|
XP_011532786.1:p.Tyr1180Cys
|
|
XR_941095.1:n.4284A>G
|
|
|
XM_011534478.3:c.4229A>G
|
XP_011532780.1:p.Tyr1410Cys
|
|
XM_011534484.2:c.3539A>G
|
XP_011532786.1:p.Tyr1180Cys
|
|
XM_017009263.1:c.*144A>G
|
XP_016864752.1:n.*144A>G
|
|
XM_017009268.1:c.3920A>G
|
XP_016864757.1:p.Tyr1307Cys
|
|
XR_001742050.2:n.4488A>G
|
|
|
NM_182925.5:c.3998A>G
MANE Select
|
NP_891555.2:p.Tyr1333Cys
|
|