ENST00000650793.2:n.507A>T
|
|
|
ENST00000697612.1:n.1185A>T
|
|
|
ENST00000374881.3:c.316A>T
|
ENSP00000364015.2:p.Asn106Tyr
|
|
ENST00000374882.8:c.328A>T
MANE Select
|
ENSP00000364016.4:p.Asn110Tyr
|
|
ENST00000650411.1:n.1649A>T
|
|
|
ENST00000650793.1:n.507A>T
|
|
|
ENST00000374881.2:c.316A>T
|
ENSP00000364015.2:p.Asn106Tyr
|
|
ENST00000374882.7:c.328A>T
|
ENSP00000364016.3:p.Asn110Tyr
|
|
ENST00000395339.7:c.296-40A>T
|
ENSP00000378748.3:n.296-40A>T
|
|
ENST00000484003.1:n.712A>T
|
|
|
NM_004159.4:c.316A>T
|
NP_004150.1:p.Asn106Tyr
|
|
NM_148919.3:c.328A>T
|
NP_683720.2:p.Asn110Tyr
|
|
NM_148919.4:c.328A>T
MANE Select
|
NP_683720.2:p.Asn110Tyr
|
|
NM_004159.5:c.316A>T
|
NP_004150.1:p.Asn106Tyr
|
|