ENST00000218099.7:c.940C>A
MANE Select
|
ENSP00000218099.2:p.His314Asn
|
|
ENST00000643157.1:n.1607C>A
|
|
|
ENST00000218099.6:c.940C>A
|
ENSP00000218099.2:p.His314Asn
|
|
ENST00000394090.2:c.826C>A
|
ENSP00000377650.2:p.His276Asn
|
|
NM_000133.3:c.940C>A , LRG_556t1:c.940C>A
|
NP_000124.1:p.His314Asn
|
|
NM_001313913.1:c.826C>A
|
NP_001300842.1:p.His276Asn
|
|
XM_005262397.3:c.811C>A
|
XP_005262454.1:p.His271Asn
|
|
XM_005262397.4:c.811C>A
|
XP_005262454.1:p.His271Asn
|
|
NM_000133.4:c.940C>A
MANE Select
|
NP_000124.1:p.His314Asn
|
|
NM_001313913.2:c.826C>A
|
NP_001300842.1:p.His276Asn
|
|