ENST00000647165.2:c.7213-59C>T
MANE Select
|
ENSP00000495481.1:n.7213-59C>T
|
|
ENST00000205890.9:c.7213-59C>T
|
ENSP00000205890.5:n.7213-59C>T
|
|
ENST00000615845.4:c.7213-59C>T
|
ENSP00000481642.1:n.7213-59C>T
|
|
NM_016239.3:c.7213-59C>T
|
NP_057323.3:n.7213-59C>T
|
|
XM_011523917.1:c.6888-59C>T
|
XP_011522219.1:n.6888-59C>T
|
|
XM_011523921.1:c.7207-59C>T
|
XP_011522223.1:n.7207-59C>T
|
|
XR_934037.1:n.7547-59C>T
|
|
|
XR_934038.1:n.7499-59C>T
|
|
|
XR_934293.1:n.434+1233G>A
|
|
|
XR_934294.1:n.435-597G>A
|
|
|
XR_934295.1:n.253+1233G>A
|
|
|
XM_017024714.2:c.7153-59C>T
|
XP_016880203.1:n.7153-59C>T
|
|
XM_017024715.2:c.7216-59C>T
|
XP_016880204.1:n.7216-59C>T
|
|
XR_934293.2:n.377+1233G>A
|
|
|
XR_934294.2:n.378-597G>A
|
|
|
NM_016239.4:c.7213-59C>T
MANE Select
|
NP_057323.3:n.7213-59C>T
|
|