ENST00000295897.9:c.1812A>G
MANE Select
|
ENSP00000295897.4:p.Gln604=
|
|
ENST00000295897.8:c.1812A>G
|
ENSP00000295897.4:p.Gln604=
|
|
ENST00000401494.7:c.1467A>G
|
ENSP00000384695.3:p.Gln489=
|
|
ENST00000415165.6:c.1236A>G
|
ENSP00000401820.2:p.Gln412=
|
|
ENST00000476441.6:c.*1091A>G
|
ENSP00000423727.1:n.*1091A>G
|
|
ENST00000495173.1:n.120A>G
|
|
|
ENST00000503124.5:c.1362A>G
|
ENSP00000421027.1:p.Gln454=
|
|
ENST00000505649.5:n.1359A>G
|
|
|
ENST00000508932.5:n.202A>G
|
|
|
ENST00000509063.5:c.1785+641A>G
|
ENSP00000422784.1:n.1785+641A>G
|
|
ENST00000511370.1:c.1345A>G
|
|
|
ENST00000621085.4:c.1173A>G
|
ENSP00000483421.1:p.Gln391=
|
|
ENST00000621628.4:c.1173A>G
|
ENSP00000480485.1:p.Gln391=
|
|
NM_000477.5:c.1812A>G
|
NP_000468.1:p.Gln604=
|
|
NM_000477.6:c.1812A>G
|
NP_000468.1:p.Gln604=
|
|
NM_000477.7:c.1812A>G
MANE Select
|
NP_000468.1:p.Gln604=
|
|