ENST00000355773.6:c.1337G>A
MANE Select
|
ENSP00000348019.5:p.Ser446Asn
|
|
ENST00000355773.5:c.1337G>A
|
ENSP00000348019.5:p.Ser446Asn
|
|
NM_012434.4:c.1337G>A
|
NP_036566.1:p.Ser446Asn
|
|
XM_005248710.2:c.1286G>A
|
XP_005248767.1:p.Ser429Asn
|
|
XM_005248711.1:c.1139G>A
|
XP_005248768.1:p.Ser380Asn
|
|
XM_011535750.1:c.1189G>A
|
XP_011534052.1:p.Val397Ile
|
|
NM_012434.5:c.1337G>A
MANE Select
|
NP_036566.1:p.Ser446Asn
|
|
NM_001382629.1:c.1106G>A
|
NP_001369558.1:p.Ser369Asn
|
|
NM_001382630.1:c.1260-5150G>A
|
NP_001369559.1:n.1260-5150G>A
|
|
NM_001382631.1:c.1358G>A
|
NP_001369560.1:p.Ser453Asn
|
|
NM_001382632.1:c.1250G>A
|
NP_001369561.1:p.Ser417Asn
|
|
NM_001382633.1:c.1337G>A
|
NP_001369562.1:p.Ser446Asn
|
|
NM_001382634.1:c.1178G>A
|
NP_001369563.1:p.Ser393Asn
|
|
NM_001382635.1:c.1334G>A
|
NP_001369564.1:p.Ser445Asn
|
|
NM_001382636.1:c.1019G>A
|
NP_001369565.1:p.Ser340Asn
|
|