ENST00000295897.9:c.1805C>G
MANE Select
|
ENSP00000295897.4:p.Ala602Gly
|
|
ENST00000295897.8:c.1805C>G
|
ENSP00000295897.4:p.Ala602Gly
|
|
ENST00000401494.7:c.1460C>G
|
ENSP00000384695.3:p.Ala487Gly
|
|
ENST00000415165.6:c.1229C>G
|
ENSP00000401820.2:p.Ala410Gly
|
|
ENST00000476441.6:c.*1084C>G
|
ENSP00000423727.1:n.*1084C>G
|
|
ENST00000495173.1:n.113C>G
|
|
|
ENST00000503124.5:c.1355C>G
|
ENSP00000421027.1:p.Ala452Gly
|
|
ENST00000505649.5:n.1352C>G
|
|
|
ENST00000508932.5:n.195C>G
|
|
|
ENST00000509063.5:c.1785+634C>G
|
ENSP00000422784.1:n.1785+634C>G
|
|
ENST00000511370.1:c.1338C>G
|
|
|
ENST00000621085.4:c.1166C>G
|
ENSP00000483421.1:p.Ala389Gly
|
|
ENST00000621628.4:c.1166C>G
|
ENSP00000480485.1:p.Ala389Gly
|
|
NM_000477.5:c.1805C>G
|
NP_000468.1:p.Ala602Gly
|
|
NM_000477.6:c.1805C>G
|
NP_000468.1:p.Ala602Gly
|
|
NM_000477.7:c.1805C>G
MANE Select
|
NP_000468.1:p.Ala602Gly
|
|