ENST00000354968.5:c.556A>T
|
ENSP00000347055.1:p.Asn186Tyr
|
|
ENST00000393450.5:c.556A>T
MANE Select
|
ENSP00000377096.1:p.Asn186Tyr
|
|
ENST00000536623.6:c.556A>T
|
ENSP00000442375.2:p.Asn186Tyr
|
|
ENST00000570671.1:c.267A>T
|
|
|
ENST00000571981.5:c.*342A>T
|
ENSP00000459035.1:n.*342A>T
|
|
ENST00000572316.5:c.556A>T
|
ENSP00000461570.1:p.Asn186Tyr
|
|
ENST00000573747.6:c.*158A>T
|
ENSP00000460734.1:n.*158A>T
|
|
NM_001002841.1:c.556A>T
|
NP_001002841.1:p.Asn186Tyr
|
|
NM_002476.2:c.556A>T
MANE Select
|
NP_002467.1:p.Asn186Tyr
|
|
XM_005257391.3:c.556A>T
|
XP_005257448.1:p.Asn186Tyr
|
|
XM_011524838.1:c.556A>T
|
XP_011523140.1:p.Asn186Tyr
|
|
XM_011524839.1:c.346A>T
|
XP_011523141.1:p.Asn116Tyr
|
|
XM_005257391.5:c.556A>T
|
XP_005257448.1:p.Asn186Tyr
|
|
XM_011524839.2:c.649A>T
|
XP_011523141.2:p.Asn217Tyr
|
|
XM_017024683.1:c.649A>T
|
XP_016880172.1:p.Asn217Tyr
|
|
XM_024450766.1:c.649A>T
|
XP_024306534.1:p.Asn217Tyr
|
|
NM_001002841.2:c.556A>T
|
NP_001002841.1:p.Asn186Tyr
|
|