ENST00000402774.8:c.657T>G
MANE Select
|
ENSP00000385990.3:p.His219Gln
|
|
ENST00000236980.10:c.657T>G
|
ENSP00000236980.6:p.His219Gln
|
|
ENST00000402774.7:c.657T>G
|
ENSP00000385990.3:p.His219Gln
|
|
ENST00000403094.3:c.657T>G
|
ENSP00000384929.3:p.His219Gln
|
|
ENST00000487777.5:n.715T>G
|
|
|
NM_001136193.1:c.657T>G
|
NP_001129665.1:p.His219Gln
|
|
NM_001136194.1:c.657T>G
|
NP_001129666.1:p.His219Gln
|
|
NM_014929.3:c.657T>G
|
NP_055744.2:p.His219Gln
|
|
NM_001136193.2:c.657T>G
MANE Select
|
NP_001129665.1:p.His219Gln
|
|
NM_001136194.2:c.657T>G
|
NP_001129666.1:p.His219Gln
|
|
NM_014929.4:c.657T>G
|
NP_055744.2:p.His219Gln
|
|