ENST00000233575.7:c.802C>G
MANE Select
|
ENSP00000233575.2:p.His268Asp
|
|
ENST00000233575.6:c.802C>G
|
ENSP00000233575.2:p.His268Asp
|
|
ENST00000427123.5:c.*612C>G
|
ENSP00000405399.1:n.*612C>G
|
|
ENST00000440760.5:c.*647C>G
|
ENSP00000399727.1:n.*647C>G
|
|
ENST00000453453.1:c.*329C>G
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ENSP00000401922.1:n.*329C>G
|
|
ENST00000493711.1:n.519C>G
|
|
|
ENST00000537606.5:c.727C>G
|
ENSP00000439208.1:p.His243Asp
|
|
NM_001267059.1:c.766C>G
|
NP_001253988.1:p.His256Asp
|
|
NM_001267060.1:c.727C>G
|
NP_001253989.1:p.His243Asp
|
|
NM_001267061.1:c.742C>G
|
NP_001253990.1:p.His248Asp
|
|
NM_014748.3:c.802C>G
|
NP_055563.1:p.His268Asp
|
|
NR_049782.1:n.1175C>G
|
|
|
NR_049783.1:n.1148C>G
|
|
|
NR_049784.1:n.1124C>G
|
|
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NR_049785.1:n.1057C>G
|
|
|
NR_049786.1:n.1006C>G
|
|
|
NR_049787.1:n.857C>G
|
|
|
NR_049788.1:n.787C>G
|
|
|
XM_011533203.1:c.160C>G
|
XP_011531505.1:p.His54Asp
|
|
XM_011533203.2:c.160C>G
|
XP_011531505.1:p.His54Asp
|
|
XM_017005405.2:c.160C>G
|
XP_016860894.1:p.His54Asp
|
|
NM_014748.4:c.802C>G
MANE Select
|
NP_055563.1:p.His268Asp
|
|
NM_001267059.2:c.766C>G
|
NP_001253988.1:p.His256Asp
|
|
NM_001267061.2:c.742C>G
|
NP_001253990.1:p.His248Asp
|
|
NR_049782.2:n.1055C>G
|
|
|
NR_049783.2:n.1028C>G
|
|
|
NR_049784.2:n.1004C>G
|
|
|
NR_049785.2:n.937C>G
|
|
|
NR_049786.2:n.886C>G
|
|
|
NR_049787.2:n.737C>G
|
|
|
NR_049788.2:n.667C>G
|
|
|
NM_001267060.2:c.727C>G
|
NP_001253989.1:p.His243Asp
|
|