ENST00000389840.7:c.1450T>G
MANE Select
|
ENSP00000374490.6:p.Ser484Ala
|
|
ENST00000389840.6:c.1450T>G
|
ENSP00000374490.6:p.Ser484Ala
|
|
ENST00000585328.5:c.1450T>G
|
ENSP00000465516.1:p.Ser484Ala
|
|
ENST00000589793.1:n.662T>G
|
|
|
NM_173628.3:c.1450T>G
|
NP_775899.3:p.Ser484Ala
|
|
XM_011525416.1:c.1450T>G
|
XP_011523718.1:p.Ser484Ala
|
|
XM_011525417.1:c.1450T>G
|
XP_011523719.1:p.Ser484Ala
|
|
XR_934583.1:n.1611T>G
|
|
|
XM_011525416.2:c.1450T>G
|
XP_011523718.1:p.Ser484Ala
|
|
XM_024451013.1:c.1450T>G
|
XP_024306781.1:p.Ser484Ala
|
|
XM_024451014.1:c.1450T>G
|
XP_024306782.1:p.Ser484Ala
|
|
XR_002958080.1:n.1613T>G
|
|
|
XR_002958081.1:n.1617T>G
|
|
|
NM_173628.4:c.1450T>G
MANE Select
|
NP_775899.3:p.Ser484Ala
|
|