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NM_000301.5:c.886T>G
MANE Select
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NP_000292.1:p.Cys296Gly
|
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ENST00000308192.14:c.886T>G
MANE Select
|
ENSP00000308938.9:p.Cys296Gly
|
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NM_000301.3:c.886T>G , LRG_571t1:c.886T>G
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NP_000292.1:p.Cys296Gly
|
|
NM_000301.4:c.886T>G
|
NP_000292.1:p.Cys296Gly
|
|
ENST00000297289.8:n.95-4016T>G
|
|
|
ENST00000297289.9:c.50-4016T>G
|
ENSP00000516619.1:n.50-4016T>G
|
|
ENST00000308192.13:c.886T>G
|
ENSP00000308938.9:p.Cys296Gly
|
|
ENST00000418964.2:c.937T>G
|
ENSP00000389424.2:p.Cys313Gly
|
|
ENST00000706906.1:c.886T>G
|
ENSP00000516618.1:p.Cys296Gly
|