ENST00000295897.9:c.1661T>G
MANE Select
|
ENSP00000295897.4:p.Val554Gly
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|
ENST00000295897.8:c.1661T>G
|
ENSP00000295897.4:p.Val554Gly
|
|
ENST00000401494.7:c.1316T>G
|
ENSP00000384695.3:p.Val439Gly
|
|
ENST00000415165.6:c.1085T>G
|
ENSP00000401820.2:p.Val362Gly
|
|
ENST00000476441.6:c.*940T>G
|
ENSP00000423727.1:n.*940T>G
|
|
ENST00000486939.1:n.315T>G
|
|
|
ENST00000503124.5:c.1211T>G
|
ENSP00000421027.1:p.Val404Gly
|
|
ENST00000505649.5:n.1208T>G
|
|
|
ENST00000508932.5:n.175+60T>G
|
|
|
ENST00000509063.5:c.1661T>G
|
ENSP00000422784.1:p.Val554Gly
|
|
ENST00000511370.1:c.1194T>G
|
|
|
ENST00000621085.4:c.1022T>G
|
ENSP00000483421.1:p.Val341Gly
|
|
ENST00000621628.4:c.1022T>G
|
ENSP00000480485.1:p.Val341Gly
|
|
NM_000477.5:c.1661T>G
|
NP_000468.1:p.Val554Gly
|
|
NM_000477.6:c.1661T>G
|
NP_000468.1:p.Val554Gly
|
|
NM_000477.7:c.1661T>G
MANE Select
|
NP_000468.1:p.Val554Gly
|
|