ENST00000480188.2:n.1451C>G
|
|
|
ENST00000696279.1:c.4737C>G
|
|
|
ENST00000696280.1:n.4506C>G
|
|
|
ENST00000696281.1:c.4435C>G
|
ENSP00000512521.1:p.Leu1479Val
|
|
ENST00000697921.1:n.3295C>G
|
|
|
ENST00000697922.1:c.*4407C>G
|
ENSP00000513478.1:n.*4407C>G
|
|
ENST00000697923.1:n.4862C>G
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|
|
ENST00000223642.3:c.4417C>G
MANE Select
|
ENSP00000223642.1:p.Leu1473Val
|
|
ENST00000223642.2:c.4417C>G
|
ENSP00000223642.1:p.Leu1473Val
|
|
NM_001735.2:c.4417C>G , LRG_28t1:c.4417C>G
|
NP_001726.2:p.Leu1473Val
|
|
XM_011518980.1:c.4432C>G
|
XP_011517282.1:p.Leu1478Val
|
|
NM_001317163.1:c.4435C>G
|
NP_001304092.1:p.Leu1479Val
|
|
NM_001317163.2:c.4435C>G
|
NP_001304092.1:p.Leu1479Val
|
|
NM_001735.3:c.4417C>G
MANE Select
|
NP_001726.2:p.Leu1473Val
|
|