ENST00000295897.9:c.1670T>G
MANE Select
|
ENSP00000295897.4:p.Val557Gly
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|
ENST00000295897.8:c.1670T>G
|
ENSP00000295897.4:p.Val557Gly
|
|
ENST00000401494.7:c.1325T>G
|
ENSP00000384695.3:p.Val442Gly
|
|
ENST00000415165.6:c.1094T>G
|
ENSP00000401820.2:p.Val365Gly
|
|
ENST00000476441.6:c.*949T>G
|
ENSP00000423727.1:n.*949T>G
|
|
ENST00000486939.1:n.324T>G
|
|
|
ENST00000503124.5:c.1220T>G
|
ENSP00000421027.1:p.Val407Gly
|
|
ENST00000505649.5:n.1217T>G
|
|
|
ENST00000508932.5:n.175+69T>G
|
|
|
ENST00000509063.5:c.1670T>G
|
ENSP00000422784.1:p.Val557Gly
|
|
ENST00000511370.1:c.1203T>G
|
|
|
ENST00000621085.4:c.1031T>G
|
ENSP00000483421.1:p.Val344Gly
|
|
ENST00000621628.4:c.1031T>G
|
ENSP00000480485.1:p.Val344Gly
|
|
NM_000477.5:c.1670T>G
|
NP_000468.1:p.Val557Gly
|
|
NM_000477.6:c.1670T>G
|
NP_000468.1:p.Val557Gly
|
|
NM_000477.7:c.1670T>G
MANE Select
|
NP_000468.1:p.Val557Gly
|
|