ENST00000272895.12:c.4606C>G
MANE Select
|
ENSP00000272895.7:p.His1536Asp
|
|
ENST00000272895.11:c.4606C>G
|
ENSP00000272895.7:p.His1536Asp
|
|
ENST00000389661.4:c.3652C>G
|
ENSP00000374312.4:p.His1218Asp
|
|
NM_015657.3:c.3652C>G
|
NP_056472.2:p.His1218Asp
|
|
NM_173076.2:c.4606C>G
|
NP_775099.2:p.His1536Asp
|
|
NR_103740.1:n.4906C>G
|
|
|
XM_011510951.1:c.4615C>G
|
XP_011509253.1:p.His1539Asp
|
|
XM_011510952.1:c.4615C>G
|
XP_011509254.1:p.His1539Asp
|
|
XM_011510951.2:c.4615C>G
|
XP_011509253.1:p.His1539Asp
|
|
NM_173076.3:c.4606C>G
MANE Select
|
NP_775099.2:p.His1536Asp
|
|
NR_103740.2:n.5104C>G
|
|
|
NM_015657.4:c.3652C>G
|
NP_056472.2:p.His1218Asp
|
|