ENST00000029410.10:c.277C>G
MANE Select
|
ENSP00000029410.5:p.His93Asp
|
|
ENST00000029410.9:c.277C>G
|
ENSP00000029410.5:p.His93Asp
|
|
ENST00000502420.1:n.256C>G
|
|
|
ENST00000505433.5:c.277C>G
|
ENSP00000425591.1:p.His93Asp
|
|
ENST00000505468.1:c.-66C>G
|
ENSP00000420886.1:n.-66C>G
|
|
ENST00000507061.1:c.94C>G
|
ENSP00000423868.1:p.His32Asp
|
|
ENST00000510761.1:c.-66C>G
|
ENSP00000423438.1:n.-66C>G
|
|
NM_007255.2:c.277C>G
|
NP_009186.1:p.His93Asp
|
|
XM_005265805.2:c.-66C>G
|
XP_005265862.1:n.-66C>G
|
|
XM_006714816.2:c.-223C>G
|
XP_006714879.1:n.-223C>G
|
|
XM_011534421.1:c.-66C>G
|
XP_011532723.1:n.-66C>G
|
|
XM_006714816.4:c.-223C>G
|
XP_006714879.1:n.-223C>G
|
|
XM_017008999.2:c.-66C>G
|
XP_016864488.1:n.-66C>G
|
|
NM_007255.3:c.277C>G
MANE Select
|
NP_009186.1:p.His93Asp
|
|