ENST00000255030.9:c.446C>T
MANE Select
|
ENSP00000255030.5:p.Ala149Val
|
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ENST00000368110.1:c.194-114C>T
|
ENSP00000357091.1:n.194-114C>T
|
|
ENST00000368111.5:c.194-114C>T
|
ENSP00000357092.1:n.194-114C>T
|
|
ENST00000368112.5:c.198-151C>T
|
ENSP00000357093.1:n.198-151C>T
|
|
ENST00000437342.1:c.-89C>T
|
ENSP00000402788.1:n.-89C>T
|
|
ENST00000473196.1:n.14C>T
|
|
|
ENST00000489317.1:n.74+253C>T
|
|
|
NM_000567.2:c.446C>T
|
NP_000558.2:p.Ala149Val
|
|
XM_011509207.1:c.446C>T
|
XP_011507509.1:p.Ala149Val
|
|
NM_001329057.1:c.446C>T
|
NP_001315986.1:p.Ala149Val
|
|
NM_001329058.1:c.198-151C>T
|
NP_001315987.1:n.198-151C>T
|
|
NM_000567.3:c.446C>T
MANE Select
|
NP_000558.2:p.Ala149Val
|
|
NM_001329057.2:c.446C>T
|
NP_001315986.1:p.Ala149Val
|
|
NM_001329058.2:c.198-151C>T
|
NP_001315987.1:n.198-151C>T
|
|
NM_001382703.1:c.194-114C>T
|
NP_001369632.1:n.194-114C>T
|
|