ENST00000366667.6:c.1251C>A
MANE Select
|
ENSP00000355627.5:p.Asn417Lys
|
|
ENST00000679738.1:c.1251C>A
|
ENSP00000505063.1:p.Asn417Lys
|
|
ENST00000679802.1:c.*710C>A
|
ENSP00000505184.1:n.*710C>A
|
|
ENST00000679854.1:n.5556C>A
|
|
|
ENST00000679957.1:c.1242C>A
|
ENSP00000506646.1:p.Asn414Lys
|
|
ENST00000680041.1:c.1251C>A
|
ENSP00000504866.1:p.Asn417Lys
|
|
ENST00000680783.1:c.829+6674C>A
|
ENSP00000506329.1:n.829+6674C>A
|
|
ENST00000681269.1:c.1251C>A
|
ENSP00000505985.1:p.Asn417Lys
|
|
ENST00000681347.1:n.3357C>A
|
|
|
ENST00000681514.1:c.1251C>A
|
ENSP00000505963.1:p.Asn417Lys
|
|
ENST00000681772.1:c.*745C>A
|
ENSP00000505829.1:n.*745C>A
|
|
ENST00000366667.4:c.1278C>A
|
ENSP00000355627.4:p.Asn426Lys
|
|
NM_000029.3:c.1278C>A
|
NP_000020.1:p.Asn426Lys
|
|
NM_000029.4:c.1278C>A
|
NP_000020.1:p.Asn426Lys
|
|
NM_001382817.3:c.1251C>A
|
NP_001369746.2:p.Asn417Lys
|
|
NM_001384479.1:c.1251C>A
MANE Select
|
NP_001371408.1:p.Asn417Lys
|
|