ENST00000281928.9:c.5011C>G
MANE Select
|
ENSP00000281928.3:p.His1671Asp
|
|
ENST00000549786.2:c.4439C>G
|
|
|
ENST00000648379.1:n.3379C>G
|
|
|
ENST00000648737.1:n.4775C>G
|
|
|
ENST00000648825.1:n.1751C>G
|
|
|
ENST00000648916.1:n.3022C>G
|
|
|
ENST00000649146.1:n.2254C>G
|
|
|
ENST00000649607.1:c.3195C>G
|
|
|
ENST00000649775.1:c.1500C>G
|
|
|
ENST00000650226.1:c.5011C>G
|
ENSP00000496981.1:p.His1671Asp
|
|
ENST00000281928.7:c.5011C>G
|
ENSP00000281928.3:p.His1671Asp
|
|
ENST00000549786.1:c.375C>G
|
|
|
ENST00000552340.1:c.43C>G
|
ENSP00000449876.1:p.His15Asp
|
|
NM_015335.4:c.5011C>G
|
NP_056150.1:p.His1671Asp
|
|
XM_011538080.1:c.5011C>G
|
XP_011536382.1:p.His1671Asp
|
|
XM_011538081.1:c.5008C>G
|
XP_011536383.1:p.His1670Asp
|
|
XM_011538082.1:c.4981C>G
|
XP_011536384.1:p.His1661Asp
|
|
XM_011538080.2:c.5011C>G
|
XP_011536382.1:p.His1671Asp
|
|
XM_011538081.2:c.5008C>G
|
XP_011536383.1:p.His1670Asp
|
|
XM_011538082.2:c.4981C>G
|
XP_011536384.1:p.His1661Asp
|
|
XM_017019090.1:c.5008C>G
|
XP_016874579.1:p.His1670Asp
|
|
NM_015335.5:c.5011C>G
MANE Select
|
NP_056150.1:p.His1671Asp
|
|