ENST00000205402.10:c.842C>T
MANE Select
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ENSP00000205402.3:p.Ala281Val
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|
ENST00000205402.9:c.842C>T
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ENSP00000205402.3:p.Ala281Val
|
|
ENST00000415325.5:c.*516C>T
|
ENSP00000402593.1:n.*516C>T
|
|
ENST00000417551.5:c.842C>T
|
ENSP00000390667.1:p.Ala281Val
|
|
ENST00000437604.6:c.698C>T
|
ENSP00000387542.2:p.Ala233Val
|
|
ENST00000440410.5:c.773C>T
|
ENSP00000417016.1:p.Ala258Val
|
|
NM_000108.4:c.842C>T
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NP_000099.2:p.Ala281Val
|
|
NM_001289750.1:c.545C>T
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NP_001276679.1:p.Ala182Val
|
|
NM_001289751.1:c.773C>T
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NP_001276680.1:p.Ala258Val
|
|
NM_001289752.1:c.698C>T
|
NP_001276681.1:p.Ala233Val
|
|
NM_000108.5:c.842C>T
MANE Select
|
NP_000099.2:p.Ala281Val
|
|