ENST00000355773.6:c.1265C>G
MANE Select
|
ENSP00000348019.5:p.Ala422Gly
|
|
ENST00000355773.5:c.1265C>G
|
ENSP00000348019.5:p.Ala422Gly
|
|
NM_012434.4:c.1265C>G
|
NP_036566.1:p.Ala422Gly
|
|
XM_005248710.2:c.1214C>G
|
XP_005248767.1:p.Ala405Gly
|
|
XM_005248711.1:c.1067C>G
|
XP_005248768.1:p.Ala356Gly
|
|
XM_011535750.1:c.1117C>G
|
XP_011534052.1:p.Leu373Val
|
|
NM_012434.5:c.1265C>G
MANE Select
|
NP_036566.1:p.Ala422Gly
|
|
NM_001382629.1:c.1034C>G
|
NP_001369558.1:p.Ala345Gly
|
|
NM_001382630.1:c.1260-5222C>G
|
NP_001369559.1:n.1260-5222C>G
|
|
NM_001382631.1:c.1286C>G
|
NP_001369560.1:p.Ala429Gly
|
|
NM_001382632.1:c.1178C>G
|
NP_001369561.1:p.Ala393Gly
|
|
NM_001382633.1:c.1265C>G
|
NP_001369562.1:p.Ala422Gly
|
|
NM_001382634.1:c.1106C>G
|
NP_001369563.1:p.Ala369Gly
|
|
NM_001382635.1:c.1262C>G
|
NP_001369564.1:p.Ala421Gly
|
|
NM_001382636.1:c.947C>G
|
NP_001369565.1:p.Ala316Gly
|
|