ENST00000327892.13:c.1242C>T
MANE Select
|
ENSP00000339001.7:p.Asn414=
|
|
ENST00000680530.1:n.2104C>T
|
|
|
ENST00000681421.1:n.2308C>T
|
|
|
ENST00000681435.1:c.1026C>T
|
ENSP00000506665.1:p.Asn342=
|
|
ENST00000327892.12:c.1242C>T
|
ENSP00000339001.7:p.Asn414=
|
|
ENST00000330914.7:c.1026C>T
|
ENSP00000365578.2:p.Asn342=
|
|
ENST00000396384.1:c.1026C>T
|
ENSP00000379668.1:p.Asn342=
|
|
ENST00000396389.5:c.1188C>T
|
ENSP00000379672.1:p.Asn396=
|
|
NM_001293212.1:c.1302C>T
|
NP_001280141.1:p.Asn434=
|
|
NM_001293213.1:c.636C>T
|
NP_001280142.1:p.Asn212=
|
|
NM_001293214.1:c.1110C>T
|
NP_001280143.1:p.Asn370=
|
|
NM_001293215.1:c.1026C>T
|
NP_001280144.1:p.Asn342=
|
|
NM_001293216.1:c.1026C>T
|
NP_001280145.1:p.Asn342=
|
|
NM_178014.3:c.1242C>T
|
NP_821133.1:p.Asn414=
|
|
NR_120608.1:n.949C>T
|
|
|
NM_178014.4:c.1242C>T
MANE Select
|
NP_821133.1:p.Asn414=
|
|
NM_001293212.2:c.1302C>T
|
NP_001280141.1:p.Asn434=
|
|
NM_001293213.2:c.636C>T
|
NP_001280142.1:p.Asn212=
|
|
NM_001293214.2:c.1110C>T
|
NP_001280143.1:p.Asn370=
|
|
NM_001293215.2:c.1026C>T
|
NP_001280144.1:p.Asn342=
|
|
NM_001293216.2:c.1026C>T
|
NP_001280145.1:p.Asn342=
|
|
NR_120608.2:n.798C>T
|
|
|