ENST00000305046.13:c.197T>A
MANE Select
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ENSP00000306606.8:p.Leu66Ter
|
|
ENST00000639454.1:c.197T>A
|
ENSP00000491622.1:p.Leu66Ter
|
|
ENST00000305046.12:c.197T>A
|
ENSP00000306606.8:p.Leu66Ter
|
|
ENST00000504498.1:n.251T>A
|
|
|
ENST00000506651.5:c.77T>A
|
ENSP00000425998.2:p.Leu26Ter
|
|
ENST00000515694.4:n.2292T>A
|
|
|
ENST00000625860.2:c.77T>A
|
ENSP00000486614.1:p.Leu26Ter
|
|
ENST00000632775.1:n.760T>A
|
|
|
NM_000668.5:c.197T>A
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NP_000659.2:p.Leu66Ter
|
|
NM_001286650.1:c.77T>A
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NP_001273579.1:p.Leu26Ter
|
|
NM_000668.6:c.197T>A
MANE Select
|
NP_000659.2:p.Leu66Ter
|
|
NM_001286650.2:c.77T>A
|
NP_001273579.1:p.Leu26Ter
|
|