ENST00000303941.4:c.1396C>G
MANE Select
|
ENSP00000306678.3:p.His466Asp
|
|
ENST00000303941.3:c.1396C>G
|
ENSP00000306678.3:p.His466Asp
|
|
NM_178510.1:c.1396C>G
|
NP_848605.1:p.His466Asp
|
|
XM_011542736.1:c.1429C>G
|
XP_011541038.1:p.His477Asp
|
|
XM_011542737.1:c.1399C>G
|
XP_011541039.1:p.His467Asp
|
|
XM_011542738.1:c.1207C>G
|
XP_011541040.1:p.His403Asp
|
|
XM_011542736.2:c.1429C>G
|
XP_011541038.1:p.His477Asp
|
|
XM_011542737.2:c.1399C>G
|
XP_011541039.1:p.His467Asp
|
|
XM_011542738.2:c.1207C>G
|
XP_011541040.1:p.His403Asp
|
|
XM_017017475.1:c.1426C>G
|
XP_016872964.1:p.His476Asp
|
|
NM_178510.2:c.1396C>G
MANE Select
|
NP_848605.1:p.His466Asp
|
|