ENST00000295897.9:c.584C>G
MANE Select
|
ENSP00000295897.4:p.Ala195Gly
|
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ENST00000295897.8:c.584C>G
|
ENSP00000295897.4:p.Ala195Gly
|
|
ENST00000401494.7:c.239C>G
|
ENSP00000384695.3:p.Ala80Gly
|
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ENST00000415165.6:c.138-2540C>G
|
ENSP00000401820.2:n.138-2540C>G
|
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ENST00000441319.5:c.590C>G
|
ENSP00000392541.1:p.Ala197Gly
|
|
ENST00000476441.6:c.181C>G
|
ENSP00000423727.1:p.Leu61Val
|
|
ENST00000503124.5:c.134C>G
|
ENSP00000421027.1:p.Ala45Gly
|
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ENST00000505649.5:n.270C>G
|
|
|
ENST00000509063.5:c.584C>G
|
ENSP00000422784.1:p.Ala195Gly
|
|
ENST00000511370.1:c.117C>G
|
|
|
ENST00000514786.1:n.553C>G
|
|
|
ENST00000621085.4:c.490+94C>G
|
ENSP00000483421.1:n.490+94C>G
|
|
ENST00000621628.4:c.486+380C>G
|
ENSP00000480485.1:n.486+380C>G
|
|
NM_000477.5:c.584C>G
|
NP_000468.1:p.Ala195Gly
|
|
NM_000477.6:c.584C>G
|
NP_000468.1:p.Ala195Gly
|
|
NM_000477.7:c.584C>G
MANE Select
|
NP_000468.1:p.Ala195Gly
|
|